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Studies of conformational changes of tubulin induced by interaction with kinesin using atomistic molecular dynamics simulations

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成果类型:
期刊论文
作者:
Shi, Xiao-Xuan;Wang, Peng-Ye;Chen, Hong;Xie, Ping
作者机构:
[Chen, Hong; Shi, Xiao-Xuan] Cent South Univ Forestry & Technol, Sch Mat Sci & Engn, Changsha 410004, Peoples R China.
[Shi, Xiao-Xuan; Wang, Peng-Ye; Xie, Ping] Chinese Acad Sci, Inst Phys, Key Lab Soft Matter Phys, Beijing 100190, Peoples R China.
语种:
英文
关键词:
adenosine diphosphate;kinesin;tubulin;kinesin;tubulin;Article;conformational transition;microtubule;molecular dynamics;protein binding;protein conformation;protein function;protein protein interaction;simulation;chemistry;metabolism;molecular dynamics;protein conformation;Adenosine Diphosphate;Kinesin;Molecular Dynamics Simulation;Protein Conformation;Tubulin
期刊:
International Journal of Molecular Sciences
ISSN:
1661-6596
年:
2021
卷:
22
期:
13
页码:
6709
基金类别:
Funding: This work was supported by the National Natural Science Foundation of China (Grant No. 11775301).
机构署名:
本校为第一机构
院系归属:
材料科学与工程学院
摘要:
The transition between strong and weak interactions of the kinesin head with the micro-tubule, which is regulated by the change of the nucleotide state of the head, is indispensable for the processive motion of the kinesin molecular motor on the microtubule. Here, using all-atom molecular dynamics simulations, the interactions between the kinesin head and tubulin are studied on the basis of the available high-resolution structural data. We found that the strong interaction can induce rapid large conformational changes of the tubulin, whereas th...

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