内在无序蛋白质
力场(虚构)
折叠(DSP实现)
分子动力学
蛋白质折叠
化学
偶极子
化学物理
生物物理学
物理
结晶学
生物系统
核磁共振
计算化学
生物
有机化学
工程类
电气工程
量子力学
作者
Yangpeng Zhang,Hao Liu,Sheng Yang,Ray Luo,Haifeng Chen
标识
DOI:10.1021/acs.jctc.9b00623
摘要
Molecular dynamics simulation as an important complement of experiment is widely used to study protein structures and functions. However, previous studies indicate that the current force fields cannot, simultaneously, provide accurate descriptions of folded proteins and intrinsically disordered proteins (IDPs). Therefore, a correction maps (CMAP)-optimized force field based on the Amber ff03 force field (termed ff03CMAP herein) was developed for a balanced sampling of folded proteins and IDPs. Extensive validations of short peptides, folded proteins, disordered proteins, and fast-folding proteins show that simulated chemical shifts, J-coupling constants, order parameters, and residual dipolar couplings (RDCs) with the ff03CMAP force field are in very good agreement with nuclear magnetic resonance measurements and are more accurate than other ff03-series force fields. The influence of solvent models was also investigated. It was found that the combination of ff03CMAP/TIP4P-Ew is suitable for folded proteins, and that of ff03CMAP/TIP4PD is better for disordered proteins. These findings confirm that the newly developed force field ff03CMAP can improve the balance of conformer sampling between folded proteins and IDPs.
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