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Lassila, Jonathan Kyle (2006-11-15) Methods for computational enzyme design and application to the chorismate-prephenate rearrangement. http://resolver.caltech.edu/CaltechETD:etd-12182006-150535


Type of Document Dissertation
Author Lassila, Jonathan Kyle
URN etd-12182006-150535
Persistent URL http://resolver.caltech.edu/CaltechETD:etd-12182006-150535
Title Methods for computational enzyme design and application to the chorismate-prephenate rearrangement
Degree PhD
Option Biochemistry and Molecular Biophysics
Advisory Committee
Advisor Name Title
Pamela Jane Bjorkman Committee Chair
Douglas C. Rees Committee Member
Frances Hamilton Arnold Committee Member
Stephen L. Mayo Committee Member
Keywords
  • site-saturation mutagenesis
  • protein-ligand interactions
  • pericyclic reactions
  • sigmatropic reactions
  • directed evolution
  • computational library design
Date of Defense 2006-11-15
Availability restricted
Abstract
The Claisen rearrangement of chorismate to prephenate has become an important model system for developing understanding of enzymatic catalysis as well as for computational treatment of enzyme active sites. This thesis presents general methods for the computational design of enzyme active sites and applies these methods to the design of catalysts for the chorismate-prephenate rearrangement. The computational methods described allow the incorporation of transition-state structures and other small molecules into protein design calculations. These design procedures were tested through redesign of the active site of Escherichia coli chorismate mutase. The six predicted mutations were experimentally characterized and most maintained or increased the catalytic activity of the enzyme. To further investigate the context of the mutations predicted in the calculation and the tolerance of a natural enzyme to secondary active site mutations, extensive substitution experiments were performed. The effect of every amino acid in five active site hydrophobic positions and one N-capping position was evaluated. These experiments clarified some of the strengths and weaknesses of the computational modeling procedure. Finally, attempts to design a completely new enzyme for catalysis of the chorismate-prephenate rearrangement are discussed.
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