Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells.
Degree: PhD, Biomedical Engineering, 2005, Georgia Tech
Detection, imaging and quantification of gene expression in living cells can provide essential information on basic biological issues and disease processes. To establish this technology, we need to develop molecular probes and cellular delivery methods to detect specific RNAs in live cells with potential for in vivo applications. In this thesis work, the major focus is placed on the development of molecular beacons and biochemical approaches (peptides etc.) to deliver such probes to different cellular compartments. These approaches are then employed to study the expression and localization of mRNAs, co-localization of mRNAs with cytoplasmic organelles and cytoskeleton, and co-localization of RNA molecules in the nuclei of living cells.
Further along this direction, we were interested in developing a better understanding of the functional states of mRNAs and the fluorescent signal observed in optical imaging experiments. To acheive this goal, we altered the translational process and studied its effect on the detection of mRNAs in living cells. The results of these studies indicate that the translational state of mRNAs favors the hybridization of molecular beacon with its target sequence. This study has also provided the evidence that molecular beacons are reversibly bound to target mRNAs and the repression of the translational process can prevent molecular beacon from binding to its target mRNA. Further, using these approaches in combination with FRAP based biophysical analysis, the dynamics of endogenous RNA in living cells are studied. These studies revealed the possible subcellular organization of RNA molecules and their dynamics in living cells. The results also demonstrated the role of cytoskeleton and ATP in the mobility of specific mRNAs in the cytoplasm.
In addition to optical probes, studies have been carried out to develop an MRI contrast agent using iron-oxide nanoparticles for deep tissue molecular imaging. Specifically, we have functionalized magnetic nanoparticles that are water-soluble, mono-dispersed, biocompatible, and easily adaptable for multifunctional bioconjugation of probes and ligands. We have successfully delivered magnetic nanoparticle bioconjugates into live cells and demonstrated their effect on relaxivity. We have further studied the role of coating thickness for optimization of contrast and further enhance the fundamental understanding of contrast mechanisms.
Advisors/Committee Members: Dr Gang Bao (Committee Chair), Dr Al Merrill (Committee Member), Dr Nicholas Hud (Committee Member), Dr Niren Murthy (Committee Member), Dr X. Hu (Committee Member).
Subjects/Keywords: Magnetic nanoparticles; RNA; MRI; Optical; Molecular beacons; Molecular imaging; RNA Detection; Nanoparticles Magnetic properties; Molecular spectroscopy; Molecular probes; Magnetic resonance imaging; Diagnostic imaging
to Zotero / EndNote / Reference
APA (6th Edition):
Nitin, N. (2005). Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7458
Chicago Manual of Style (16th Edition):
Nitin, Nitin. “Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells.” 2005. Doctoral Dissertation, Georgia Tech. Accessed December 04, 2020.
MLA Handbook (7th Edition):
Nitin, Nitin. “Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells.” 2005. Web. 04 Dec 2020.
Nitin N. Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2020 Dec 04].
Available from: http://hdl.handle.net/1853/7458.
Council of Science Editors:
Nitin N. Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7458