Optimized protein-water interactions and torsional refinements yield balanced atomistic protein force fields

Tien Minh Phan (), Priyesh Mohanty and Jeetain Mittal ()
Additional contact information
Tien Minh Phan: Texas A&M University, Artie McFerrin Department of Chemical Engineering
Priyesh Mohanty: Texas A&M University, Artie McFerrin Department of Chemical Engineering
Jeetain Mittal: Texas A&M University, Artie McFerrin Department of Chemical Engineering

Nature Communications, 2025, vol. 16, issue 1, 1-15

Abstract: Abstract All-atom molecular dynamics (MD) simulations based on physics-based force fields serve as an essential complement to experiments for investigating protein structure, dynamics, and interactions. Despite significant advances in force field parameterization, achieving a consistent balance of molecular interactions that stabilize folded proteins while accurately capturing the conformational dynamics of intrinsically disordered polypeptides in solution remains challenging. In this work, we introduce two refined force fields which incorporate either a selective upscaling of protein-water interactions or targeted improvements to backbone torsional sampling: (i) amber ff03w-sc, and (ii) amber ff99SBws-STQ′. Extensive validation against small-angle X-ray scattering (SAXS) and nuclear magnetic resonance (NMR) spectroscopy observables revealed that both force fields accurately reproduced the chain dimensions and secondary structure propensities of IDPs. Importantly, both force fields also maintained the stability of single-chain folded proteins and protein-protein complexes over microsecond-timescale simulations. Overall, our refinement strategies result in transferable force fields with improved accuracy for simulating diverse protein systems, ranging from folded domains to IDPs and protein-protein complexes.

Date: 2025
References: Add references at CitEc
Citations:

Downloads: (external link)
https://www.nature.com/articles/s41467-025-65603-4 Abstract (text/html)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-65603-4

Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/

DOI: 10.1038/s41467-025-65603-4

Access Statistics for this article

Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie

More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().