Title page for ETD etd-10072005-094901


Type of Document Master's Thesis
Author Kurusu, Tamaki
URN etd-10072005-094901
Title Computer simulation of free energies to predict cis/trans equilibria of prolyl peptides and solvation free energies of phenylalanyl peptides
Degree Master of Science
Department Biochemistry
Advisory Committee
Advisor Name Title
Bevan, David R. Committee Chair
Gregory, Eugene M. Committee Member
Newton, William E. Committee Member
Keywords
  • Molecular Modeling
  • Simulation
  • Free Energy
  • Proline
  • Solvation
  • PeptideTwo computer simulation studies were perfor
  • the free energy perturbation (FEP) method
  • using AMBER
  • was utilized to calculate the Gibbs free energy di
  • from which the ratio of cis to trans conformers wa
  • our results were encouraging in that they predicte
  • compared to Ace-Asn-Pro-NMe
  • which agrees with experimental results. Part II ap
Date of Defense 1996-08-05
Availability restricted
Abstract
Two computer simulation studies were performed; one to help understand the structure-function relationships of prolyl peptides (Part I) and the other to help predict more efficient pharmaceutical drug delivery by molecular modification of small peptides (Part II).

In Part I, the free energy perturbation (FEP) method, using AMBER, was utilized to calculate the Gibbs free energy difference between cis and trans conformers of Ace-Tyr-Pro- NMe and Ace-Asn-Pro-NMe, from which the ratio of cis to trans conformers was obtained. Our simulation generated much lower %cis for both peptides as compared with experimental values and possible problems in our computational schemes are presented. However, our results were encouraging in that they predicted preference of trans conformers for both peptides and higher %cis for Ace-Tyr-Pro-NMe, compared to Ace-Asn-Pro-NMe, which agrees with experimental results.

Part II applied semi empirical (AMS0L) and microscopic simulation (POLARIS) methods to obtain the solvation free energies of a series of phenylalanyl peptides with various degrees of methylation on their backbone nitrogens. It was clearly predicted that as a peptide length increased, so solvation free energy decreased, indicating less favorable permeability through the cell membrane system, in agreement with data in the literature. AMSOL also showed that solvation free energy change upon methylation was variable depending on the position of the substituted backbone nitrogen, which disagrees with the literature. However, non-systematic solvation free energy change of small amines upon methylation was successfully predicted by AMSOL, in good accord with experimental data.

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