力场(虚构)
二面角
分子动力学
磷酸化
内在无序蛋白质
伞式取样
分子力学
化学
生物物理学
化学物理
纳米技术
材料科学
计算化学
物理
分子
生物化学
生物
氢键
有机化学
量子力学
作者
Ge Song,Bozitao Zhong,Bo Zhang,Ashfaq Ur Rehman,Haifeng Chen
标识
DOI:10.1021/acs.jcim.3c00112
摘要
Phosphorylation of proteins plays an important regulatory role at almost all levels of cellular organization. Molecular dynamics (MD) simulation is a promising tool to reveal the mechanism of how phosphorylation regulates many key biological processes at the atomistic level. MD simulation accuracy depends on force field precision, while the current force fields for phospho-amino acids have resulted in notable inconsistency with experimental data. Here, a new force field parameter (named FB18CMAP) is generated by fitting against quantum mechanics (QM) energy in aqueous solution with φ/ψ dihedral potential-energy surfaces optimized using CMAP parameters. MD simulations of phosphorylated dipeptides, intrinsically disordered proteins (IDPs), and ordered (folded) proteins show that FB18CMAP can mimic NMR observables and structural characteristics of phosphorylated dipeptides and proteins more accurately than the FB18 force field. These findings suggest that FB18CMAP performs well in both the simulation of ordered and disordered states of phosphorylated proteins.
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