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Force field development in protein design

Citation

Zollars, Eric Stafford (2006) Force field development in protein design. Dissertation (Ph.D.), California Institute of Technology. http://resolver.caltech.edu/CaltechETD:etd-06052006-155305

Abstract

Protein design requires the rapid evaluation of very large numbers of equations during the course of a calculation. These equations must represent the important contributors to protein stability in simple and accurate terms. Some physical phenomena are relatively easy to model such as van der Waals forces. Electrostatics and solvation in a protein environment are forces that are more difficult to adequately capture. Additionally, the balance of the terms used must be determined in order to design sequences that fold to stable, specific folds.

The electrostatic interactions within the protein and between the protein and solvent are important in both the stability and function of the protein. The effects of the protein-solvent interactions are evaluated using implicit models that consider the solvent as a bulk. These interactions are quantified using the Poisson-Boltzmann equation that must be solved using discrete numerical methods. We sought to avoid this performance hit by scaling a simpler model of electrostatics, Coulomb's law, to reproduce one aspect of the protein-solvent interaction: solvent screening. By dividing the Coulombic dielectric into two parts and scaling to correlate with the Poisson-Boltzmann results we significantly increased the strength of electrostatics in our force field that led to the design of a more stable engrailed homeodomain.

The second part of this work describes attempts to reparameterize our protein design force field. Many protein mutants have been expressed and biophysically characterized in the literature. We sought to use the measured stabilities of protein mutants in the literature to balance the terms in the force field. While we were able to produce a force field that could reproduce experimental energies, this force field led to unsatisfactory designed sequences. To more fully satisfy the unique conditions of a protein design force field we explored other optimization techniques and found that the balance of the terms in the existing force field is nearly optima

Item Type:Thesis (Dissertation (Ph.D.))
Subject Keywords:electrostatics; force field; optimization; protein design
Degree Grantor:California Institute of Technology
Division:Biology
Major Option:Biochemistry and Molecular Biophysics
Thesis Availability:Restricted to Caltech community only
Research Advisor(s):
  • Mayo, Stephen L.
Thesis Committee:
  • Pierce, Niles A. (chair)
  • Rees, Douglas C.
  • Bjorkman, Pamela J.
  • Mayo, Stephen L.
Defense Date:25 May 2006
Record Number:CaltechETD:etd-06052006-155305
Persistent URL:http://resolver.caltech.edu/CaltechETD:etd-06052006-155305
Default Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:2464
Collection:CaltechTHESIS
Deposited By: Imported from ETD-db
Deposited On:05 Jun 2006
Last Modified:26 Dec 2012 02:51

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