Statistical models of protein conformational dynamics

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Abstract/Contents

Abstract
Understanding the conformational dynamics of biological macromolecules at atomic resolution remains a grand challenge at the intersection of biology, chemistry, and physics. Molecular dynamics (MD) --- which refers to computational simulations of the atomic-level interactions and equations of motions that give rise to these dynamics --- is a powerful approach that now produces immense quantities of time series data on the dynamics of these systems. Here, I describe a variety of new methodologies for analyzing the rare events in these MD data sets in an automatic, statically-sound manner, and constructing the appropriate simplified models of these processes. These techniques are rooted in the theory of reversible Markov chains. They include new classes of Markov state models, hidden Markov models, and reaction coordinate finding algorithms, with applications to protein folding and conformational change. A particular focus herein is on methods for model selection and model comparison, and computationally efficient algorithms.

Description

Type of resource text
Form electronic; electronic resource; remote
Extent 1 online resource.
Publication date 2016
Issuance monographic
Language English

Creators/Contributors

Associated with McGibbon, Robert T
Associated with Stanford University, Department of Chemistry.
Primary advisor Pande, Vijay
Thesis advisor Pande, Vijay
Thesis advisor Markland, Thomas E
Thesis advisor Martinez, Todd J. (Todd Joseph), 1968-
Advisor Markland, Thomas E
Advisor Martinez, Todd J. (Todd Joseph), 1968-

Subjects

Genre Theses

Bibliographic information

Statement of responsibility Robert T. McGibbon.
Note Submitted to the Department of Chemistry.
Thesis Thesis (Ph.D.)--Stanford University, 2016.
Location electronic resource

Access conditions

Copyright
© 2016 by Robert Treiman McGibbon
License
This work is licensed under a Creative Commons Attribution 3.0 Unported license (CC BY).

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