Force Field Effects in Simulations of Flexible Peptides with Varying Polyproline II Propensity.

ABSTRACT: Five peptides previously suggested to possess polyproline II (PPII) structure have here been investigated by using atomistic molecular dynamics simulations to compare how well four different force fields known for simulating intrinsically disordered proteins relatively well (Amber ff99SB-disp, Amber ff99SB-ILDN, CHARM36IDPSFF, and CHARMM36m) can capture this secondary structure element. The results revealed that all force fields sample PPII structures but to different extents and with different propensities toward other secondary structure elements, in particular, the β-sheet and "random coils". A cluster analysis of the simulations of histatin 5 also revealed that the conformational ensembles of the force fields are quite different. We compared the simulations to circular dichroism and nu

SUBMITTER: Jephthah S 

PROVIDER: S-EPMC8515809 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature