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You searched for subject:(Protein membrane interactions). Showing records 1 – 30 of 61 total matches.

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Hong Kong University of Science and Technology

1. Wu, Min. A preliminary characterization of neuroligin interacting proteins.

Degree: 2014, Hong Kong University of Science and Technology

 Neuroligins are cell adhesion molecules on the postsynaptic membrane that associate with their presynaptic partners, neurexins. The trans-synaptic neuroligin-neurexin interaction has been extensively investigated in… (more)

Subjects/Keywords: Membrane proteins; Protein-protein interactions

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APA (6th Edition):

Wu, M. (2014). A preliminary characterization of neuroligin interacting proteins. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1333501 ; http://repository.ust.hk/ir/bitstream/1783.1-87515/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wu, Min. “A preliminary characterization of neuroligin interacting proteins.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed August 19, 2019. https://doi.org/10.14711/thesis-b1333501 ; http://repository.ust.hk/ir/bitstream/1783.1-87515/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wu, Min. “A preliminary characterization of neuroligin interacting proteins.” 2014. Web. 19 Aug 2019.

Vancouver:

Wu M. A preliminary characterization of neuroligin interacting proteins. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Aug 19]. Available from: https://doi.org/10.14711/thesis-b1333501 ; http://repository.ust.hk/ir/bitstream/1783.1-87515/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wu M. A preliminary characterization of neuroligin interacting proteins. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1333501 ; http://repository.ust.hk/ir/bitstream/1783.1-87515/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Boston College

2. He, Tao. I. Exploration of Amphitropic Protein Interactions at the Membrane Interface; II. DNF2—A Plant Protein with Homology to Bacterial PI-PLC Enzymes.

Degree: PhD, Chemistry, 2015, Boston College

 Amphitropic proteins, such as the virulence factor phosphatidylinositol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis, often depend on lipid-specific recognition of target membranes. However, the recognition… (more)

Subjects/Keywords: cation-π interactions; protein-membrane interactions

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APA (6th Edition):

He, T. (2015). I. Exploration of Amphitropic Protein Interactions at the Membrane Interface; II. DNF2—A Plant Protein with Homology to Bacterial PI-PLC Enzymes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104815

Chicago Manual of Style (16th Edition):

He, Tao. “I. Exploration of Amphitropic Protein Interactions at the Membrane Interface; II. DNF2—A Plant Protein with Homology to Bacterial PI-PLC Enzymes.” 2015. Doctoral Dissertation, Boston College. Accessed August 19, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104815.

MLA Handbook (7th Edition):

He, Tao. “I. Exploration of Amphitropic Protein Interactions at the Membrane Interface; II. DNF2—A Plant Protein with Homology to Bacterial PI-PLC Enzymes.” 2015. Web. 19 Aug 2019.

Vancouver:

He T. I. Exploration of Amphitropic Protein Interactions at the Membrane Interface; II. DNF2—A Plant Protein with Homology to Bacterial PI-PLC Enzymes. [Internet] [Doctoral dissertation]. Boston College; 2015. [cited 2019 Aug 19]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104815.

Council of Science Editors:

He T. I. Exploration of Amphitropic Protein Interactions at the Membrane Interface; II. DNF2—A Plant Protein with Homology to Bacterial PI-PLC Enzymes. [Doctoral Dissertation]. Boston College; 2015. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104815


The Ohio State University

3. Nair, Manoj Sadasivan. Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes.

Degree: PhD, Biophysics, 2008, The Ohio State University

  The most controversial step in the study of the mechanism of action of insecticidal crystal toxins is that of insertion of the toxin into… (more)

Subjects/Keywords: Biochemistry; Biophysics; Entomology; Microbiology; Molecular Biology; Toxicology; Biophysics; Protein-protein interactions; Protein-lipid interactions; Protein oligomerization; Membrane insertion; Toxin- membrane interactions

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APA (6th Edition):

Nair, M. S. (2008). Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470

Chicago Manual of Style (16th Edition):

Nair, Manoj Sadasivan. “Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes.” 2008. Doctoral Dissertation, The Ohio State University. Accessed August 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470.

MLA Handbook (7th Edition):

Nair, Manoj Sadasivan. “Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes.” 2008. Web. 19 Aug 2019.

Vancouver:

Nair MS. Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2019 Aug 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470.

Council of Science Editors:

Nair MS. Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470


Cornell University

4. Richards, Mark. Investigating Lipid-Protein Interactions Using Supported Lipid Bilayers .

Degree: 2016, Cornell University

Membrane proteins play vital roles in cell function and as such represent the targets of over 60% of pharmaceuticals on the market1. Lipid interactions with… (more)

Subjects/Keywords: Membrane proteins; Lipid-Protein Interactions; Lipid Bilayers

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APA (6th Edition):

Richards, M. (2016). Investigating Lipid-Protein Interactions Using Supported Lipid Bilayers . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/43676

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Richards, Mark. “Investigating Lipid-Protein Interactions Using Supported Lipid Bilayers .” 2016. Thesis, Cornell University. Accessed August 19, 2019. http://hdl.handle.net/1813/43676.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Richards, Mark. “Investigating Lipid-Protein Interactions Using Supported Lipid Bilayers .” 2016. Web. 19 Aug 2019.

Vancouver:

Richards M. Investigating Lipid-Protein Interactions Using Supported Lipid Bilayers . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/1813/43676.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Richards M. Investigating Lipid-Protein Interactions Using Supported Lipid Bilayers . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/43676

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Minnesota

5. Smith, Elizabeth. Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins.

Degree: PhD, Physics, 2015, University of Minnesota

 The interactions of peripheral membrane proteins with both membrane lipids and proteins are vital for many cellular processes including membrane trafficking, cellular signaling, and cell… (more)

Subjects/Keywords: brightness; fluorescence; peripheral membrane protein; protein-lipid interactions; protein-protein interactions; z-scan

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APA (6th Edition):

Smith, E. (2015). Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174893

Chicago Manual of Style (16th Edition):

Smith, Elizabeth. “Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins.” 2015. Doctoral Dissertation, University of Minnesota. Accessed August 19, 2019. http://hdl.handle.net/11299/174893.

MLA Handbook (7th Edition):

Smith, Elizabeth. “Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins.” 2015. Web. 19 Aug 2019.

Vancouver:

Smith E. Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/11299/174893.

Council of Science Editors:

Smith E. Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/174893

6. Sjöhamn, Jennie. Human Aquaporins: Production, Characterization and Interactions.

Degree: 2015, University of Gothenburg / Göteborgs Universitet

Membrane proteins are essential components of the cell and responsible for the communication with the outside environment and transport of molecules across the membrane. Water… (more)

Subjects/Keywords: aquaporins; membrane protein; protein production; protein characterization; protein:protein interactions; structural biochemistry

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APA (6th Edition):

Sjöhamn, J. (2015). Human Aquaporins: Production, Characterization and Interactions. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/40589

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sjöhamn, Jennie. “Human Aquaporins: Production, Characterization and Interactions.” 2015. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed August 19, 2019. http://hdl.handle.net/2077/40589.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sjöhamn, Jennie. “Human Aquaporins: Production, Characterization and Interactions.” 2015. Web. 19 Aug 2019.

Vancouver:

Sjöhamn J. Human Aquaporins: Production, Characterization and Interactions. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2015. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/2077/40589.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sjöhamn J. Human Aquaporins: Production, Characterization and Interactions. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2015. Available from: http://hdl.handle.net/2077/40589

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oxford

7. Naughton, Fiona. Interactions of perihperal membrane proteins with phosphatidylinositol lipids : insights from molecular dynamics simulations.

Degree: PhD, 2017, University of Oxford

Interactions between proteins and membranes are central to many signalling pathways and other cellular processes. Phosphatidylinositol phosphates (PIPs) are a family of lipids often acting… (more)

Subjects/Keywords: Protein-membrane interactions; Molecular dynamics; Peripheral membrane proteins; Phosphatidylinositol phosphate lipids

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APA (6th Edition):

Naughton, F. (2017). Interactions of perihperal membrane proteins with phosphatidylinositol lipids : insights from molecular dynamics simulations. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:d7bb7b03-3eda-40f2-85fc-f5a314ae3c44 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740945

Chicago Manual of Style (16th Edition):

Naughton, Fiona. “Interactions of perihperal membrane proteins with phosphatidylinositol lipids : insights from molecular dynamics simulations.” 2017. Doctoral Dissertation, University of Oxford. Accessed August 19, 2019. https://ora.ox.ac.uk/objects/uuid:d7bb7b03-3eda-40f2-85fc-f5a314ae3c44 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740945.

MLA Handbook (7th Edition):

Naughton, Fiona. “Interactions of perihperal membrane proteins with phosphatidylinositol lipids : insights from molecular dynamics simulations.” 2017. Web. 19 Aug 2019.

Vancouver:

Naughton F. Interactions of perihperal membrane proteins with phosphatidylinositol lipids : insights from molecular dynamics simulations. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2019 Aug 19]. Available from: https://ora.ox.ac.uk/objects/uuid:d7bb7b03-3eda-40f2-85fc-f5a314ae3c44 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740945.

Council of Science Editors:

Naughton F. Interactions of perihperal membrane proteins with phosphatidylinositol lipids : insights from molecular dynamics simulations. [Doctoral Dissertation]. University of Oxford; 2017. Available from: https://ora.ox.ac.uk/objects/uuid:d7bb7b03-3eda-40f2-85fc-f5a314ae3c44 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740945


Texas A&M University

8. Draheim, Roger Russell. The role of protein-membrane interactions in modulation of signaling by bacterial chemoreceptors.

Degree: 2009, Texas A&M University

 Environmental signals are sensed by membrane-spanning receptors that communicate with the cell interior. Bacterial chemoreceptors modulate the activity of the CheA kinase in response to… (more)

Subjects/Keywords: membrane-protein interactions; receptors; signal transduction; two-component systems; protein engineering

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APA (6th Edition):

Draheim, R. R. (2009). The role of protein-membrane interactions in modulation of signaling by bacterial chemoreceptors. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1336

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Draheim, Roger Russell. “The role of protein-membrane interactions in modulation of signaling by bacterial chemoreceptors.” 2009. Thesis, Texas A&M University. Accessed August 19, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-1336.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Draheim, Roger Russell. “The role of protein-membrane interactions in modulation of signaling by bacterial chemoreceptors.” 2009. Web. 19 Aug 2019.

Vancouver:

Draheim RR. The role of protein-membrane interactions in modulation of signaling by bacterial chemoreceptors. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1336.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Draheim RR. The role of protein-membrane interactions in modulation of signaling by bacterial chemoreceptors. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1336

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universiteit Utrecht

9. Meijneke, T. Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides.

Degree: 2010, Universiteit Utrecht

Membrane protein research is an important, but problem-riddled field. One method to obtain knowledge on this class of proteins is by studying the molecular mechanisms… (more)

Subjects/Keywords: Scheikunde; membrane protein; WALP; model peptide; protein-lipid interactions; helix-helix

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APA (6th Edition):

Meijneke, T. (2010). Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/179898

Chicago Manual of Style (16th Edition):

Meijneke, T. “Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides.” 2010. Doctoral Dissertation, Universiteit Utrecht. Accessed August 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/179898.

MLA Handbook (7th Edition):

Meijneke, T. “Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides.” 2010. Web. 19 Aug 2019.

Vancouver:

Meijneke T. Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2010. [cited 2019 Aug 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/179898.

Council of Science Editors:

Meijneke T. Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides. [Doctoral Dissertation]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/179898


Princeton University

10. McCabe, Anne Louise. Regulation of the Beta-barrel Assembly Machine complex in Escherichia coli .

Degree: PhD, 2017, Princeton University

 The outer membrane of Escherichia coli functions as a selectively permeable barrier between the bacterium and its external environment, allowing for the influx of ions… (more)

Subjects/Keywords: Escherichia coli; Gram-negative bacteria; membrane biogenesis; outer membrane proteins; protein-protein interactions

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APA (6th Edition):

McCabe, A. L. (2017). Regulation of the Beta-barrel Assembly Machine complex in Escherichia coli . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01xk81jp031

Chicago Manual of Style (16th Edition):

McCabe, Anne Louise. “Regulation of the Beta-barrel Assembly Machine complex in Escherichia coli .” 2017. Doctoral Dissertation, Princeton University. Accessed August 19, 2019. http://arks.princeton.edu/ark:/88435/dsp01xk81jp031.

MLA Handbook (7th Edition):

McCabe, Anne Louise. “Regulation of the Beta-barrel Assembly Machine complex in Escherichia coli .” 2017. Web. 19 Aug 2019.

Vancouver:

McCabe AL. Regulation of the Beta-barrel Assembly Machine complex in Escherichia coli . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Aug 19]. Available from: http://arks.princeton.edu/ark:/88435/dsp01xk81jp031.

Council of Science Editors:

McCabe AL. Regulation of the Beta-barrel Assembly Machine complex in Escherichia coli . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01xk81jp031


Penn State University

11. Gill, Richard Lee. Insight Into the Molecular Mechanisms of Membrane Geometry Generation and Recognition.

Degree: PhD, Biochemistry and Molecular Biology, 2014, Penn State University

Membrane remodeling is an essential process in cell growth, division, intracellular vesicle transport, and many other essential biological phenomena. Furthermore, membrane geometry has recently been… (more)

Subjects/Keywords: Structural Biology; Protein-Lipid Interactions; NMR; Membrane Curvature Sensing

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APA (6th Edition):

Gill, R. L. (2014). Insight Into the Molecular Mechanisms of Membrane Geometry Generation and Recognition. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/25690

Chicago Manual of Style (16th Edition):

Gill, Richard Lee. “Insight Into the Molecular Mechanisms of Membrane Geometry Generation and Recognition.” 2014. Doctoral Dissertation, Penn State University. Accessed August 19, 2019. https://etda.libraries.psu.edu/catalog/25690.

MLA Handbook (7th Edition):

Gill, Richard Lee. “Insight Into the Molecular Mechanisms of Membrane Geometry Generation and Recognition.” 2014. Web. 19 Aug 2019.

Vancouver:

Gill RL. Insight Into the Molecular Mechanisms of Membrane Geometry Generation and Recognition. [Internet] [Doctoral dissertation]. Penn State University; 2014. [cited 2019 Aug 19]. Available from: https://etda.libraries.psu.edu/catalog/25690.

Council of Science Editors:

Gill RL. Insight Into the Molecular Mechanisms of Membrane Geometry Generation and Recognition. [Doctoral Dissertation]. Penn State University; 2014. Available from: https://etda.libraries.psu.edu/catalog/25690


UCLA

12. Lee, Michelle. Unified Mechanisms of Membrane Curvature Generation by Diverse Peptides and Proteins.

Degree: Biomedical Engineering, 2017, UCLA

 A diverse range of biologically critical phenomena involve membrane remodeling and/or the induction of membrane curvature changes by peptides or proteins. These events require a… (more)

Subjects/Keywords: Biomedical engineering; Biophysics; curvature; interactions; membrane; peptide; protein

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APA (6th Edition):

Lee, M. (2017). Unified Mechanisms of Membrane Curvature Generation by Diverse Peptides and Proteins. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/04b9w0mw

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Michelle. “Unified Mechanisms of Membrane Curvature Generation by Diverse Peptides and Proteins.” 2017. Thesis, UCLA. Accessed August 19, 2019. http://www.escholarship.org/uc/item/04b9w0mw.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Michelle. “Unified Mechanisms of Membrane Curvature Generation by Diverse Peptides and Proteins.” 2017. Web. 19 Aug 2019.

Vancouver:

Lee M. Unified Mechanisms of Membrane Curvature Generation by Diverse Peptides and Proteins. [Internet] [Thesis]. UCLA; 2017. [cited 2019 Aug 19]. Available from: http://www.escholarship.org/uc/item/04b9w0mw.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee M. Unified Mechanisms of Membrane Curvature Generation by Diverse Peptides and Proteins. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/04b9w0mw

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

13. Gajsiewicz, Joshua M. Polyphosphate and tissue factor/factor VIIA as initiators of coagulation.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

Protein-membrane interactions are a critical component of the coagulation cascade. For many coagulation factors, these interactions are mediated via γ-carboxyglutamate rich regions, or GLA domains,… (more)

Subjects/Keywords: Blood coagulation; Clotting; Protein-membrane interactions; Tissue factor (TF); Polyphosphate

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APA (6th Edition):

Gajsiewicz, J. M. (2016). Polyphosphate and tissue factor/factor VIIA as initiators of coagulation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95553

Chicago Manual of Style (16th Edition):

Gajsiewicz, Joshua M. “Polyphosphate and tissue factor/factor VIIA as initiators of coagulation.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 19, 2019. http://hdl.handle.net/2142/95553.

MLA Handbook (7th Edition):

Gajsiewicz, Joshua M. “Polyphosphate and tissue factor/factor VIIA as initiators of coagulation.” 2016. Web. 19 Aug 2019.

Vancouver:

Gajsiewicz JM. Polyphosphate and tissue factor/factor VIIA as initiators of coagulation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/2142/95553.

Council of Science Editors:

Gajsiewicz JM. Polyphosphate and tissue factor/factor VIIA as initiators of coagulation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95553


University of Illinois – Urbana-Champaign

14. Boettcher, John M. NMR investigations of blood coagulation: Conformational changes of membrane bilayers and proteins in blood coagulation.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 A multitude of biological processes involve membranes and their associated membrane proteins. The interactions of these biological molecules lead to perturbations in their structure and… (more)

Subjects/Keywords: membrane proteins; protein interactions; biological Nuclear magnetic resonance (NMR)

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APA (6th Edition):

Boettcher, J. M. (2010). NMR investigations of blood coagulation: Conformational changes of membrane bilayers and proteins in blood coagulation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15550

Chicago Manual of Style (16th Edition):

Boettcher, John M. “NMR investigations of blood coagulation: Conformational changes of membrane bilayers and proteins in blood coagulation.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 19, 2019. http://hdl.handle.net/2142/15550.

MLA Handbook (7th Edition):

Boettcher, John M. “NMR investigations of blood coagulation: Conformational changes of membrane bilayers and proteins in blood coagulation.” 2010. Web. 19 Aug 2019.

Vancouver:

Boettcher JM. NMR investigations of blood coagulation: Conformational changes of membrane bilayers and proteins in blood coagulation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/2142/15550.

Council of Science Editors:

Boettcher JM. NMR investigations of blood coagulation: Conformational changes of membrane bilayers and proteins in blood coagulation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15550


University of Rochester

15. Horn, Joshua N. Exploring Lipid-Peptide Interactions Through Computer Simulation of Antimicrobial Lipopeptides and a G Protein-Coupled Receptor.

Degree: PhD, 2013, University of Rochester

 Phospholipid bilayers are critical components of living organisms. They organize into membranes that encapsulate the contents of cells and organelles, compartmentalizing cellular function and separating… (more)

Subjects/Keywords: Molecular Dynamics; Simulation; Lipopeptides; Rhodopsin; Membrane; Lipids; Lipid-Protein Interactions

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APA (6th Edition):

Horn, J. N. (2013). Exploring Lipid-Peptide Interactions Through Computer Simulation of Antimicrobial Lipopeptides and a G Protein-Coupled Receptor. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27875

Chicago Manual of Style (16th Edition):

Horn, Joshua N. “Exploring Lipid-Peptide Interactions Through Computer Simulation of Antimicrobial Lipopeptides and a G Protein-Coupled Receptor.” 2013. Doctoral Dissertation, University of Rochester. Accessed August 19, 2019. http://hdl.handle.net/1802/27875.

MLA Handbook (7th Edition):

Horn, Joshua N. “Exploring Lipid-Peptide Interactions Through Computer Simulation of Antimicrobial Lipopeptides and a G Protein-Coupled Receptor.” 2013. Web. 19 Aug 2019.

Vancouver:

Horn JN. Exploring Lipid-Peptide Interactions Through Computer Simulation of Antimicrobial Lipopeptides and a G Protein-Coupled Receptor. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/1802/27875.

Council of Science Editors:

Horn JN. Exploring Lipid-Peptide Interactions Through Computer Simulation of Antimicrobial Lipopeptides and a G Protein-Coupled Receptor. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27875


North Carolina State University

16. Choi, Ucheor B. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.

Degree: PhD, Physics, 2010, North Carolina State University

 Conformational information about proteins can often reveal the mechanisms of their biological functions. This thesis examines conformational aspects of the synaptic SNARE (soluble N-ethylmaleimide-sensitive factor… (more)

Subjects/Keywords: protein-protein interactions; synaptic vesicle; single molecule FRET; neurotransmitter release; membrane fusion

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APA (6th Edition):

Choi, U. B. (2010). Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/6220

Chicago Manual of Style (16th Edition):

Choi, Ucheor B. “Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.” 2010. Doctoral Dissertation, North Carolina State University. Accessed August 19, 2019. http://www.lib.ncsu.edu/resolver/1840.16/6220.

MLA Handbook (7th Edition):

Choi, Ucheor B. “Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.” 2010. Web. 19 Aug 2019.

Vancouver:

Choi UB. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. [Internet] [Doctoral dissertation]. North Carolina State University; 2010. [cited 2019 Aug 19]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6220.

Council of Science Editors:

Choi UB. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. [Doctoral Dissertation]. North Carolina State University; 2010. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6220


University of Toronto

17. Edwards, Michelle. In Situ Mapping of Membranolytic Protein-membrane Interactions by Combined Attenuated Total Reflection Fourier-transform Infrared Spectroscopy-atomic Force Microscopy (ATR-FTIR-AFM).

Degree: 2011, University of Toronto

A combined attenuated total reflection-Fourier-transform infrared spectroscopy (ATR-FTIR)-atomic force microscopy (AFM) platform was used to visualize and characterize membranolytic protein- and peptide-membrane interactions, allowing spectroscopic… (more)

Subjects/Keywords: atomic force microscopy; infrared spectroscopy; protein-membrane interactions; peptide-membrane interactions; sticholysin; cationic antimicrobial peptide; 0786; 0541

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APA (6th Edition):

Edwards, M. (2011). In Situ Mapping of Membranolytic Protein-membrane Interactions by Combined Attenuated Total Reflection Fourier-transform Infrared Spectroscopy-atomic Force Microscopy (ATR-FTIR-AFM). (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30585

Chicago Manual of Style (16th Edition):

Edwards, Michelle. “In Situ Mapping of Membranolytic Protein-membrane Interactions by Combined Attenuated Total Reflection Fourier-transform Infrared Spectroscopy-atomic Force Microscopy (ATR-FTIR-AFM).” 2011. Masters Thesis, University of Toronto. Accessed August 19, 2019. http://hdl.handle.net/1807/30585.

MLA Handbook (7th Edition):

Edwards, Michelle. “In Situ Mapping of Membranolytic Protein-membrane Interactions by Combined Attenuated Total Reflection Fourier-transform Infrared Spectroscopy-atomic Force Microscopy (ATR-FTIR-AFM).” 2011. Web. 19 Aug 2019.

Vancouver:

Edwards M. In Situ Mapping of Membranolytic Protein-membrane Interactions by Combined Attenuated Total Reflection Fourier-transform Infrared Spectroscopy-atomic Force Microscopy (ATR-FTIR-AFM). [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/1807/30585.

Council of Science Editors:

Edwards M. In Situ Mapping of Membranolytic Protein-membrane Interactions by Combined Attenuated Total Reflection Fourier-transform Infrared Spectroscopy-atomic Force Microscopy (ATR-FTIR-AFM). [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30585


University of Pennsylvania

18. Shi, Zheng. Mechanisms of Membrane Remodeling by Peripheral Proteins and Divalent Cations.

Degree: 2015, University of Pennsylvania

 Biological membranes undergo constant shape remodeling involving the formation of highly curved structures. As one of the most extensively studied membrane remodeling events, endocytosis is… (more)

Subjects/Keywords: alpha Synuclein; BAR domain proteins; Divalent cations; Membrane curvature; Membrane dynamics; Protein membrane interactions; Biophysics; Chemistry; Physical Chemistry

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APA (6th Edition):

Shi, Z. (2015). Mechanisms of Membrane Remodeling by Peripheral Proteins and Divalent Cations. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2011

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Shi, Zheng. “Mechanisms of Membrane Remodeling by Peripheral Proteins and Divalent Cations.” 2015. Thesis, University of Pennsylvania. Accessed August 19, 2019. https://repository.upenn.edu/edissertations/2011.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Shi, Zheng. “Mechanisms of Membrane Remodeling by Peripheral Proteins and Divalent Cations.” 2015. Web. 19 Aug 2019.

Vancouver:

Shi Z. Mechanisms of Membrane Remodeling by Peripheral Proteins and Divalent Cations. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2019 Aug 19]. Available from: https://repository.upenn.edu/edissertations/2011.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Shi Z. Mechanisms of Membrane Remodeling by Peripheral Proteins and Divalent Cations. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/2011

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


National University of Ireland – Galway

19. Eriksson, Emma Sofia Elisabeth. Computational Studies of Hypericin and Porphyrin Derivatives for Photodynamic Therapy - Spectra, Membrane Simulations, and Protein Interactions .

Degree: 2011, National University of Ireland – Galway

 Photosensitizing compounds with potential application in anticancer treatment with photodynamic therapy were investigated by means of computational methods in the studies presented in this thesis.… (more)

Subjects/Keywords: Computational studies; Hypericin; Porphyrin; Photodynamic therapy; Spectra; Membrane simulations; Protein interactions; Chemistry

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APA (6th Edition):

Eriksson, E. S. E. (2011). Computational Studies of Hypericin and Porphyrin Derivatives for Photodynamic Therapy - Spectra, Membrane Simulations, and Protein Interactions . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/2613

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Eriksson, Emma Sofia Elisabeth. “Computational Studies of Hypericin and Porphyrin Derivatives for Photodynamic Therapy - Spectra, Membrane Simulations, and Protein Interactions .” 2011. Thesis, National University of Ireland – Galway. Accessed August 19, 2019. http://hdl.handle.net/10379/2613.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Eriksson, Emma Sofia Elisabeth. “Computational Studies of Hypericin and Porphyrin Derivatives for Photodynamic Therapy - Spectra, Membrane Simulations, and Protein Interactions .” 2011. Web. 19 Aug 2019.

Vancouver:

Eriksson ESE. Computational Studies of Hypericin and Porphyrin Derivatives for Photodynamic Therapy - Spectra, Membrane Simulations, and Protein Interactions . [Internet] [Thesis]. National University of Ireland – Galway; 2011. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/10379/2613.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Eriksson ESE. Computational Studies of Hypericin and Porphyrin Derivatives for Photodynamic Therapy - Spectra, Membrane Simulations, and Protein Interactions . [Thesis]. National University of Ireland – Galway; 2011. Available from: http://hdl.handle.net/10379/2613

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Waterloo

20. Ignagni, Nicholas. Engineering Applications of Surface Plasmon Resonance: Protein–Protein and Protein–Molecule Interactions.

Degree: 2011, University of Waterloo

Protein-protein and protein-molecule interactions are complicated phenomena due to the tendency of proteins to change shape and function in response to their environment. Protein aggregation… (more)

Subjects/Keywords: Surface Plasmon Resonance; SPR; Adsorption; protein; Beta Lactoglobulin; interactions; kinetics; membrane fouling

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APA (6th Edition):

Ignagni, N. (2011). Engineering Applications of Surface Plasmon Resonance: Protein–Protein and Protein–Molecule Interactions. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/6294

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ignagni, Nicholas. “Engineering Applications of Surface Plasmon Resonance: Protein–Protein and Protein–Molecule Interactions.” 2011. Thesis, University of Waterloo. Accessed August 19, 2019. http://hdl.handle.net/10012/6294.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ignagni, Nicholas. “Engineering Applications of Surface Plasmon Resonance: Protein–Protein and Protein–Molecule Interactions.” 2011. Web. 19 Aug 2019.

Vancouver:

Ignagni N. Engineering Applications of Surface Plasmon Resonance: Protein–Protein and Protein–Molecule Interactions. [Internet] [Thesis]. University of Waterloo; 2011. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/10012/6294.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ignagni N. Engineering Applications of Surface Plasmon Resonance: Protein–Protein and Protein–Molecule Interactions. [Thesis]. University of Waterloo; 2011. Available from: http://hdl.handle.net/10012/6294

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Minnesota

21. Csizmar, Clifford. Engineered Proteins for Studying and Controlling Cellular Recognition.

Degree: PhD, Medicinal Chemistry, 2018, University of Minnesota

 The ability to direct cell-cell interactions has tremendous value in several therapeutic fields. While genetically-encoded artificial receptors have proven efficacious, their scope is limited by… (more)

Subjects/Keywords: Avidity; Cell-Cell Interactions; Cell Membrane Engineering; Nanotechnology; Protein Engineering; Targeted Therapeutics

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APA (6th Edition):

Csizmar, C. (2018). Engineered Proteins for Studying and Controlling Cellular Recognition. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/201057

Chicago Manual of Style (16th Edition):

Csizmar, Clifford. “Engineered Proteins for Studying and Controlling Cellular Recognition.” 2018. Doctoral Dissertation, University of Minnesota. Accessed August 19, 2019. http://hdl.handle.net/11299/201057.

MLA Handbook (7th Edition):

Csizmar, Clifford. “Engineered Proteins for Studying and Controlling Cellular Recognition.” 2018. Web. 19 Aug 2019.

Vancouver:

Csizmar C. Engineered Proteins for Studying and Controlling Cellular Recognition. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/11299/201057.

Council of Science Editors:

Csizmar C. Engineered Proteins for Studying and Controlling Cellular Recognition. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/201057


University of Hong Kong

22. Gao, Wei. Characterization of protein interactors of Arabidopsis acyl-coenzymea-binding protein 2.

Degree: PhD, 2009, University of Hong Kong

published_or_final_version

Biological Sciences

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Chye, ML.

Subjects/Keywords: Membrane proteins.; Arabidopsis thaliana.; Protein-protein interactions.; Acetylcoenzyme A.

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APA (6th Edition):

Gao, W. (2009). Characterization of protein interactors of Arabidopsis acyl-coenzymea-binding protein 2. (Doctoral Dissertation). University of Hong Kong. Retrieved from Gao, W. [高威]. (2009). Characterization of protein interactors of Arabidopsis acyl-coenzyme a-binding protein 2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322383 ; http://dx.doi.org/10.5353/th_b4322383 ; http://hdl.handle.net/10722/130798

Chicago Manual of Style (16th Edition):

Gao, Wei. “Characterization of protein interactors of Arabidopsis acyl-coenzymea-binding protein 2.” 2009. Doctoral Dissertation, University of Hong Kong. Accessed August 19, 2019. Gao, W. [高威]. (2009). Characterization of protein interactors of Arabidopsis acyl-coenzyme a-binding protein 2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322383 ; http://dx.doi.org/10.5353/th_b4322383 ; http://hdl.handle.net/10722/130798.

MLA Handbook (7th Edition):

Gao, Wei. “Characterization of protein interactors of Arabidopsis acyl-coenzymea-binding protein 2.” 2009. Web. 19 Aug 2019.

Vancouver:

Gao W. Characterization of protein interactors of Arabidopsis acyl-coenzymea-binding protein 2. [Internet] [Doctoral dissertation]. University of Hong Kong; 2009. [cited 2019 Aug 19]. Available from: Gao, W. [高威]. (2009). Characterization of protein interactors of Arabidopsis acyl-coenzyme a-binding protein 2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322383 ; http://dx.doi.org/10.5353/th_b4322383 ; http://hdl.handle.net/10722/130798.

Council of Science Editors:

Gao W. Characterization of protein interactors of Arabidopsis acyl-coenzymea-binding protein 2. [Doctoral Dissertation]. University of Hong Kong; 2009. Available from: Gao, W. [高威]. (2009). Characterization of protein interactors of Arabidopsis acyl-coenzyme a-binding protein 2. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4322383 ; http://dx.doi.org/10.5353/th_b4322383 ; http://hdl.handle.net/10722/130798


University of Arkansas

23. Rankenberg, Johanna Maria. Tryptophan Anchored Peptides in Lipid Bilayer Membranes: Control of Peptide Orientation and the Phase Behavior of Cholesterol-Containing Ternary Lipid Mixtures.

Degree: PhD, 2010, University of Arkansas

  Model WALP peptides and "next generation" WALP-derived hydrophobic model peptides were employed to discover principles that govern protein-lipid interactions in biological membranes. Ternary cholesterol-containing… (more)

Subjects/Keywords: Pure sciences; Biological sciences; Cholesterol; Lipid bilayer membranes; Membrane lipid interactions; Membrane protein interactions; Peptide orientation; Phase behavior; Ternary lipid mixtures; Tryptophan anchored peptides; Biochemistry; Biophysics

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APA (6th Edition):

Rankenberg, J. M. (2010). Tryptophan Anchored Peptides in Lipid Bilayer Membranes: Control of Peptide Orientation and the Phase Behavior of Cholesterol-Containing Ternary Lipid Mixtures. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/196

Chicago Manual of Style (16th Edition):

Rankenberg, Johanna Maria. “Tryptophan Anchored Peptides in Lipid Bilayer Membranes: Control of Peptide Orientation and the Phase Behavior of Cholesterol-Containing Ternary Lipid Mixtures.” 2010. Doctoral Dissertation, University of Arkansas. Accessed August 19, 2019. https://scholarworks.uark.edu/etd/196.

MLA Handbook (7th Edition):

Rankenberg, Johanna Maria. “Tryptophan Anchored Peptides in Lipid Bilayer Membranes: Control of Peptide Orientation and the Phase Behavior of Cholesterol-Containing Ternary Lipid Mixtures.” 2010. Web. 19 Aug 2019.

Vancouver:

Rankenberg JM. Tryptophan Anchored Peptides in Lipid Bilayer Membranes: Control of Peptide Orientation and the Phase Behavior of Cholesterol-Containing Ternary Lipid Mixtures. [Internet] [Doctoral dissertation]. University of Arkansas; 2010. [cited 2019 Aug 19]. Available from: https://scholarworks.uark.edu/etd/196.

Council of Science Editors:

Rankenberg JM. Tryptophan Anchored Peptides in Lipid Bilayer Membranes: Control of Peptide Orientation and the Phase Behavior of Cholesterol-Containing Ternary Lipid Mixtures. [Doctoral Dissertation]. University of Arkansas; 2010. Available from: https://scholarworks.uark.edu/etd/196


Indian Institute of Science

24. Mondal, Somnath. Structural and Dynamic Studies of Protein-Nanomaterial Interactions.

Degree: 2016, Indian Institute of Science

 My thesis is divided into five chapters, starting with a general introduction in first chapter and sample preparation and protein-NMR assignment techniques in second chapter.… (more)

Subjects/Keywords: Structural Proteins; Protein-Nanomaterial Interactions; Nanomaterials; Protein-NMR; Carbon Quantum Dots; Ubiquitin-Graphene Oxide Interactions; NMR Spectroscopy; Macromolecular Crowding; Membrane Proteins; Intrinisically Disordered Proteins; Protein Structure; Protein Stability; Nanobiotechnology; Macromolecular Crowder; L-hIGFBP2; Protein Graphene Oxide interactions; Solid State Chemistry

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APA (6th Edition):

Mondal, S. (2016). Structural and Dynamic Studies of Protein-Nanomaterial Interactions. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2823

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mondal, Somnath. “Structural and Dynamic Studies of Protein-Nanomaterial Interactions.” 2016. Thesis, Indian Institute of Science. Accessed August 19, 2019. http://hdl.handle.net/2005/2823.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mondal, Somnath. “Structural and Dynamic Studies of Protein-Nanomaterial Interactions.” 2016. Web. 19 Aug 2019.

Vancouver:

Mondal S. Structural and Dynamic Studies of Protein-Nanomaterial Interactions. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Aug 19]. Available from: http://hdl.handle.net/2005/2823.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mondal S. Structural and Dynamic Studies of Protein-Nanomaterial Interactions. [Thesis]. Indian Institute of Science; 2016. Available from: http://hdl.handle.net/2005/2823

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

25. Mondal, Somnath. Structural and Dynamic Studies of Protein-Nanomaterial Interactions.

Degree: 2016, Indian Institute of Science

 My thesis is divided into five chapters, starting with a general introduction in first chapter and sample preparation and protein-NMR assignment techniques in second chapter.… (more)

Subjects/Keywords: Structural Proteins; Protein-Nanomaterial Interactions; Nanomaterials; Protein-NMR; Carbon Quantum Dots; Ubiquitin-Graphene Oxide Interactions; NMR Spectroscopy; Macromolecular Crowding; Membrane Proteins; Intrinisically Disordered Proteins; Protein Structure; Protein Stability; Nanobiotechnology; Macromolecular Crowder; L-hIGFBP2; Protein Graphene Oxide interactions; Solid State Chemistry

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APA (6th Edition):

Mondal, S. (2016). Structural and Dynamic Studies of Protein-Nanomaterial Interactions. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2823 ; http://etd.ncsi.iisc.ernet.in/abstracts/3673/G27873-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mondal, Somnath. “Structural and Dynamic Studies of Protein-Nanomaterial Interactions.” 2016. Thesis, Indian Institute of Science. Accessed August 19, 2019. http://etd.iisc.ernet.in/handle/2005/2823 ; http://etd.ncsi.iisc.ernet.in/abstracts/3673/G27873-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mondal, Somnath. “Structural and Dynamic Studies of Protein-Nanomaterial Interactions.” 2016. Web. 19 Aug 2019.

Vancouver:

Mondal S. Structural and Dynamic Studies of Protein-Nanomaterial Interactions. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Aug 19]. Available from: http://etd.iisc.ernet.in/handle/2005/2823 ; http://etd.ncsi.iisc.ernet.in/abstracts/3673/G27873-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mondal S. Structural and Dynamic Studies of Protein-Nanomaterial Interactions. [Thesis]. Indian Institute of Science; 2016. Available from: http://etd.iisc.ernet.in/handle/2005/2823 ; http://etd.ncsi.iisc.ernet.in/abstracts/3673/G27873-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

26. Mardoukhi Rohani, Mahsa. EFFECT OF ELECTROSTATIC INTERACTIONS DURING PROTEIN ULTRAFILTRATION: EFFECTS OF LIGAND CHEMISTRY AND PROTEIN SURFACE CHARGE DISTRIBUTION.

Degree: PhD, Chemical Engineering, 2011, Penn State University

 The production of high value recombinant proteins requires robust, cost-effective, and high-resolution purification methods that can provide high yield and purification. Although ultrafiltration (UF) was… (more)

Subjects/Keywords: Ultrafiltration; Electrostatic Interactions; Membrane Filtration; Protein

…including the electrostatic interactions between the charged protein and membrane. The earliest… …Charge Distribution on Electrostatic Interactions during Protein Ultrafiltration… …interaction for a positively charged protein in a positively charged membrane. Conditions: rs = 1.59… …densities for the protein and membrane) for the zwitterionic membranes. Filled symbols… …charged UltracelTM membrane as a function of the net protein charge determined from the measured… 

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APA (6th Edition):

Mardoukhi Rohani, M. (2011). EFFECT OF ELECTROSTATIC INTERACTIONS DURING PROTEIN ULTRAFILTRATION: EFFECTS OF LIGAND CHEMISTRY AND PROTEIN SURFACE CHARGE DISTRIBUTION. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/12519

Chicago Manual of Style (16th Edition):

Mardoukhi Rohani, Mahsa. “EFFECT OF ELECTROSTATIC INTERACTIONS DURING PROTEIN ULTRAFILTRATION: EFFECTS OF LIGAND CHEMISTRY AND PROTEIN SURFACE CHARGE DISTRIBUTION.” 2011. Doctoral Dissertation, Penn State University. Accessed August 19, 2019. https://etda.libraries.psu.edu/catalog/12519.

MLA Handbook (7th Edition):

Mardoukhi Rohani, Mahsa. “EFFECT OF ELECTROSTATIC INTERACTIONS DURING PROTEIN ULTRAFILTRATION: EFFECTS OF LIGAND CHEMISTRY AND PROTEIN SURFACE CHARGE DISTRIBUTION.” 2011. Web. 19 Aug 2019.

Vancouver:

Mardoukhi Rohani M. EFFECT OF ELECTROSTATIC INTERACTIONS DURING PROTEIN ULTRAFILTRATION: EFFECTS OF LIGAND CHEMISTRY AND PROTEIN SURFACE CHARGE DISTRIBUTION. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2019 Aug 19]. Available from: https://etda.libraries.psu.edu/catalog/12519.

Council of Science Editors:

Mardoukhi Rohani M. EFFECT OF ELECTROSTATIC INTERACTIONS DURING PROTEIN ULTRAFILTRATION: EFFECTS OF LIGAND CHEMISTRY AND PROTEIN SURFACE CHARGE DISTRIBUTION. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/12519


Kent State University

27. Putta, Priya. The Tale/ Head of Two Membrane Lipids Through Protein Interactions.

Degree: PhD, College of Arts and Sciences / Department of Biological Sciences, 2018, Kent State University

 Plants are versatile and diverse photosynthetic eukaryotes. They adapt and flourish in every corner of the earth. Plants have been a vital part of human… (more)

Subjects/Keywords: Biochemistry; Biology; Molecular Biology; Cellular Biology; Phosphatidic acid; Diacylglycerol Pyrophoshpate; Membrane lipids; Lipid-Protein Interactions; plant stress proteins

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Putta, P. (2018). The Tale/ Head of Two Membrane Lipids Through Protein Interactions. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1524311387080992

Chicago Manual of Style (16th Edition):

Putta, Priya. “The Tale/ Head of Two Membrane Lipids Through Protein Interactions.” 2018. Doctoral Dissertation, Kent State University. Accessed August 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1524311387080992.

MLA Handbook (7th Edition):

Putta, Priya. “The Tale/ Head of Two Membrane Lipids Through Protein Interactions.” 2018. Web. 19 Aug 2019.

Vancouver:

Putta P. The Tale/ Head of Two Membrane Lipids Through Protein Interactions. [Internet] [Doctoral dissertation]. Kent State University; 2018. [cited 2019 Aug 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1524311387080992.

Council of Science Editors:

Putta P. The Tale/ Head of Two Membrane Lipids Through Protein Interactions. [Doctoral Dissertation]. Kent State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1524311387080992


Universiteit Utrecht

28. Cabukusta, B. HOW TO HUNT FOR INTERACTION PARTNERS OF MEMBRANE PROTEINS IN VIVO?.

Degree: 2012, Universiteit Utrecht

Membrane proteins consist approximately 30% of the genes of an average organism and they are critical for several cell functions, such as signaling, energy transduction… (more)

Subjects/Keywords: membrane proteins; protein-protein interactions; ppi; yeast two-hybrid system; translational machinery; photo-crosslinking amino acids; orthogonal tRNA; orthogonal aminoacyl-tRNA synthetase

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cabukusta, B. (2012). HOW TO HUNT FOR INTERACTION PARTNERS OF MEMBRANE PROTEINS IN VIVO?. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/255188

Chicago Manual of Style (16th Edition):

Cabukusta, B. “HOW TO HUNT FOR INTERACTION PARTNERS OF MEMBRANE PROTEINS IN VIVO?.” 2012. Masters Thesis, Universiteit Utrecht. Accessed August 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/255188.

MLA Handbook (7th Edition):

Cabukusta, B. “HOW TO HUNT FOR INTERACTION PARTNERS OF MEMBRANE PROTEINS IN VIVO?.” 2012. Web. 19 Aug 2019.

Vancouver:

Cabukusta B. HOW TO HUNT FOR INTERACTION PARTNERS OF MEMBRANE PROTEINS IN VIVO?. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2019 Aug 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/255188.

Council of Science Editors:

Cabukusta B. HOW TO HUNT FOR INTERACTION PARTNERS OF MEMBRANE PROTEINS IN VIVO?. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/255188

29. Meijneke, T. Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides.

Degree: 2010, University Utrecht

Membrane protein research is an important, but problem-riddled field. One method to obtain knowledge on this class of proteins is by studying the molecular mechanisms… (more)

Subjects/Keywords: membrane protein; WALP; model peptide; protein-lipid interactions; helix-helix

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Meijneke, T. (2010). Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/179898 ; URN:NBN:NL:UI:10-1874-179898 ; urn:isbn:978-90-393-5392-9 ; URN:NBN:NL:UI:10-1874-179898 ; http://dspace.library.uu.nl/handle/1874/179898

Chicago Manual of Style (16th Edition):

Meijneke, T. “Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides.” 2010. Doctoral Dissertation, University Utrecht. Accessed August 19, 2019. http://dspace.library.uu.nl/handle/1874/179898 ; URN:NBN:NL:UI:10-1874-179898 ; urn:isbn:978-90-393-5392-9 ; URN:NBN:NL:UI:10-1874-179898 ; http://dspace.library.uu.nl/handle/1874/179898.

MLA Handbook (7th Edition):

Meijneke, T. “Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides.” 2010. Web. 19 Aug 2019.

Vancouver:

Meijneke T. Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides. [Internet] [Doctoral dissertation]. University Utrecht; 2010. [cited 2019 Aug 19]. Available from: http://dspace.library.uu.nl/handle/1874/179898 ; URN:NBN:NL:UI:10-1874-179898 ; urn:isbn:978-90-393-5392-9 ; URN:NBN:NL:UI:10-1874-179898 ; http://dspace.library.uu.nl/handle/1874/179898.

Council of Science Editors:

Meijneke T. Towards a better understanding of membrane proteins : Synthesis and biophysical characterization of oligomeric model peptides. [Doctoral Dissertation]. University Utrecht; 2010. Available from: http://dspace.library.uu.nl/handle/1874/179898 ; URN:NBN:NL:UI:10-1874-179898 ; urn:isbn:978-90-393-5392-9 ; URN:NBN:NL:UI:10-1874-179898 ; http://dspace.library.uu.nl/handle/1874/179898

30. MADHUBRATA GHOSH. LIPID AND NUCLEOTIDE-MEDIATED ALLOSTERY IN SIGNALING PROTEINS.

Degree: 2016, National University of Singapore

Subjects/Keywords: hydrogen deuterium exchange; mass spectrometry; allostery; membrane proteins; protein-ligand interactions; protein-lipid interactions

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

GHOSH, M. (2016). LIPID AND NUCLEOTIDE-MEDIATED ALLOSTERY IN SIGNALING PROTEINS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/134970

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

GHOSH, MADHUBRATA. “LIPID AND NUCLEOTIDE-MEDIATED ALLOSTERY IN SIGNALING PROTEINS.” 2016. Thesis, National University of Singapore. Accessed August 19, 2019. http://scholarbank.nus.edu.sg/handle/10635/134970.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

GHOSH, MADHUBRATA. “LIPID AND NUCLEOTIDE-MEDIATED ALLOSTERY IN SIGNALING PROTEINS.” 2016. Web. 19 Aug 2019.

Vancouver:

GHOSH M. LIPID AND NUCLEOTIDE-MEDIATED ALLOSTERY IN SIGNALING PROTEINS. [Internet] [Thesis]. National University of Singapore; 2016. [cited 2019 Aug 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/134970.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

GHOSH M. LIPID AND NUCLEOTIDE-MEDIATED ALLOSTERY IN SIGNALING PROTEINS. [Thesis]. National University of Singapore; 2016. Available from: http://scholarbank.nus.edu.sg/handle/10635/134970

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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