| Literature DB >> 33591749 |
Junxi Mu1, Hao Liu1, Jian Zhang2, Ray Luo3, Hai-Feng Chen1.
Abstract
Intrinsically disordered proteins (IDPs) are widely distributed across eukaryotic cells, playing important roles in molecular recognition, molecular assembly, post-translational modification, and other biological processes. IDPs are also associated with many diseases such as cancers, cardiovascular diseases, and neurodegenerative diseases. Due to their structural flexibility, conventional experimental methods cannot reliably capture their heterogeneous structures. Molecular dynamics simulation becomes an important complementary tool to quantify IDP structures. This review covers recent force field strategies proposed for more accurate molecular dynamics simulations of IDPs. The strategies include adjusting dihedral parameters, adding grid-based energy correction map (CMAP) parameters, refining protein-water interactions, and others. Different force fields were found to perform well on specific observables of specific IDPs but also are limited in reproducing all available experimental observables consistently for all tested IDPs. We conclude the review with perspective areas for improvements for future force fields for IDPs.Entities:
Keywords: AMBER; CHARMM; CMAP; Dihedral parameters; Force field; GROMOS; Intrinsically disordered proteins; Molecular simulations; OPSL-AA
Year: 2021 PMID: 33591749 PMCID: PMC8256680 DOI: 10.1021/acs.jcim.0c01175
Source DB: PubMed Journal: J Chem Inf Model ISSN: 1549-9596 Impact factor: 4.956