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ABSINTH: A new continuum solvation model for simulations of polypeptides in aqueous solutions
Author(s) -
Vitalis Andreas,
Pappu Rohit V.
Publication year - 2008
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.21005
Subject(s) - solvation , implicit solvation , chemistry , force field (fiction) , aqueous solution , solvent models , computational chemistry , monte carlo method , chemical physics , molecular dynamics , solvent , folding (dsp implementation) , thermodynamics , physics , organic chemistry , quantum mechanics , statistics , mathematics , electrical engineering , engineering
A new implicit solvation model for use in Monte Carlo simulations of polypeptides is introduced. The model is termed ABSINTH for self‐ A ssembly of B iomolecules S tudied by an I mplicit, N ovel, and T unable H amiltonian. It is designed primarily for simulating conformational equilibria and oligomerization reactions of intrinsically disordered proteins in aqueous solutions. The paradigm for ABSINTH is conceptually similar to the EEF1 model of Lazaridis and Karplus (Proteins 1999, 35, 133). In ABSINTH, the transfer of a polypeptide solute from the gas phase into a continuum solvent is the sum of a direct mean field interaction (DMFI), and a term to model the screening of polar interactions. Polypeptide solutes are decomposed into a set of distinct solvation groups. The DMFI is a sum of contributions from each of the solvation groups, which are analogs of model compounds. Continuum‐mediated screening of electrostatic interactions is achieved using a framework similar to the one used for the DMFI. Promising results are shown for a set of test cases. These include the calculation of NMR coupling constants for short peptides, the assessment of the thermal stability of two small proteins, reversible folding of both an α‐helix and a β‐hairpin forming peptide, and the polymeric properties of intrinsically disordered polyglutamine peptides of varying lengths. The tests reveal that the computational expense for simulations with the ABSINTH implicit solvation model increase by a factor that is in the range of 2.5–5.0 with respect to gas‐phase calculations. © 2008 Wiley Periodicals, Inc. J Comput Chem, 2009