Common structural transitions in explicit-solvent simulations of villin headpiece folding.

ABSTRACT: Molecular dynamics simulations of protein folding can provide very high-resolution data on the folding process; however, due to computational challenges most studies of protein folding have been limited to small peptides, or made use of approximations such as Gō potentials or implicit solvent models. We have performed a set of molecular dynamics simulations totaling >50 micros on the villin headpiece subdomain, one of the most stable and fastest-folding naturally occurring proteins, in explicit solvent. We find that the wild-type villin headpiece reliably folds to a native conformation on timescales similar to experimentally observed folding, but that a fast folding double-norleucine mutant shows significantly more heterogeneous behavior. Along with other recent simulation studies, we note

SUBMITTER: Freddolino PL 

PROVIDER: S-EPMC2764099 | biostudies-literature | 2009 Oct

REPOSITORIES: biostudies-literature