Superfunneled Energy Landscape of Protein Evolution Unifies the Principles of Protein Evolution, Folding, and Design

被引:8
作者
Yan, Zhiqiang [1 ]
Wang, Jin [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Elect Chem, Changchun 130022, Jilin, Peoples R China
[2] SUNY Stony Brook, Dept Chem & Phys, Stony Brook, NY 11790 USA
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
COARSE-GRAINED MODELS; VILLIN HEADPIECE; THERMODYNAMIC STABILITY; STATISTICAL-MECHANICS; CRYSTAL-STRUCTURES; LATTICE-MODEL; CORE-PACKING; WW DOMAIN; SEQUENCE; DESIGNABILITY;
D O I
10.1103/PhysRevLett.122.018103
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Evolution is essential for shaping the biological functions. Darwin proposed the selection as the driving force for evolution upon mutations. While mutations are clear, the quantification of the selection force is still challenging. In this study, we identified and quantified both thermodynamic stability and kinetic accessibility as the selection forces for protein evolution. The protein evolution can be viewed and quantified as a trajectory moving along a superfunneled energy landscape with a line attractor at the bottom. The resulting evolved sequences and structures show strong protein characteristics including the hydrophobic core, high designability, and fast folding. The evolution principle uncovered here is validated on real proteins and sheds light on the protein design.
引用
收藏
页数:7
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