pKa Shifts in Small Molecules and HIV Protease: Electrostatics and Conformation

Published

June 24, 1998

Author(s)

R Luo, M S. Head, J Moult, M K. Gilson

Abstract

The generalized Born [GB] approximation is a reasonable electrostatic model that is fast enough for use with extensive conformational sampling. This study combines the GB model with a torsion-space sampling method to compute pK_a shifts for a series of dicarboxylic acids and amino acids, and for the active-site aspartyl dyad in HIV-1 protease. The calculations agree rather well with experiment for the small molecules. Conformational analysis shows salt-bridging for the zwitterionic amino acids but otherwise modest electrostatic effects upon mean chain-lengths. The calculations also show that through-space electrical fields alone cannot account completely for the observed pK_a shifts. The calculations for HIV protease agree reasonably well with experiment, despite the complexity of the system. The present computational approach should be useful for a variety of other applications.

Citation

Journal of the American Chemical Society

Volume

120

Issue

24

Pub Type

Journals

Keywords

electrostatic, free energy, generalized born, HIV protease, salt bridge

Citation

Luo, R. , Head, M. , Moult, J. and Gilson, M. (1998), pK_a Shifts in Small Molecules and HIV Protease: Electrostatics and Conformation, Journal of the American Chemical Society (Accessed March 5, 2025)