Doctoral Dissertations
Date of Award
8-2021
Degree Type
Dissertation
Degree Name
Doctor of Philosophy
Major
Life Sciences
Major Professor
Tongye Shen
Committee Members
Tongye Shen, Sandrasegaram Gnanakaran, Rachel P. McCord, Elias J. Fernandez, Hong Guo
Abstract
Many proteins undergo conformational switching in order to perform their cellular functions. A multitude of factors may shift the energy landscape and alter protein dynamics with varying effects on the conformations they explore. We apply atomistic molecular dynamics simulations to a variety of biomolecular systems in order to investigate how factors such as pressure, the chemical environment, and ligand binding at distant binding pockets affect the structure and dynamics of these protein systems. Further, we examine how such changes should be characterized. We first investigate how pressure and solvent modulate ligand access to the active site of a bacterial lipase by probing the dynamics in a variety of pressures and DMSO-water solvent mixtures. By measuring the gorge leading to the binding pocket we find small amounts of DMSO and high atmospheric pressure optimize the ability of lipids to reach the catalytic interior. Next, we examine the allosteric mechanism behind cooperative and anti-cooperative binding of nuclear hormone receptor RXR and two of its binding partners (TR and CAR). We detail why ligands of the RXR:TR (9c and t3) complex bind anti-cooperatively while ligands of RXR:CAR (9c and tcp) bind cooperatively. Finally, we describe how an intrinsically disordered protein, α-synuclein, alters its conformational dynamics in a pH-dependent manner increasing the likelihood of pathogenic aggregation and neurodegenerative disease at low pH. In each case, we apply contact analysis to uncover the collective motions underlying conformational change triggered by environmental factors or ligand binding.
Recommended Citation
Lindsay, Richard J., "MODULATION OF PROTEIN DYNAMICS BY LIGAND BINDING AND SOLVENT COMPOSITION. " PhD diss., University of Tennessee, 2021.
https://trace.tennessee.edu/utk_graddiss/6566