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通过原子模拟表征原核旋转A-ATP酶外周柄的柔韧性

Characterization of the flexibility of the peripheral stalk of prokaryotic rotary A-ATPases by atomistic simulations.

作者信息

Papachristos Kostas, Muench Stephen P, Paci Emanuele

机构信息

Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, England.

School of Molecular and Cellular Biology, University of Leeds, Leeds, England.

出版信息

Proteins. 2016 Sep;84(9):1203-12. doi: 10.1002/prot.25066. Epub 2016 Jun 1.

Abstract

Rotary ATPases are involved in numerous physiological processes, with the three distinct types (F/A/V-ATPases) sharing functional properties and structural features. The basic mechanism involves the counter rotation of two motors, a soluble ATP hydrolyzing/synthesizing domain and a membrane-embedded ion pump connected through a central rotor axle and a stator complex. Within the A/V-ATPase family conformational flexibility of the EG stators has been shown to accommodate catalytic cycling and is considered to be important to function. For the A-ATPase three EG structures have been reported, thought to represent conformational states of the stator during different stages of rotary catalysis. Here we use long, detailed atomistic simulations to show that those structures are conformers explored through thermal fluctuations, but do not represent highly populated states of the EG stator in solution. We show that the coiled coil tail domain has a high persistence length (∼100 nm), but retains the ability to adapt to different conformational states through the presence of two hinge regions. Moreover, the stator network of the related V-ATPase has been suggested to adapt to subunit interactions in the collar region in addition to the nucleotide occupancy of the catalytic domain. The MD simulations reported here, reinforce this observation showing that the EG stators have enough flexibility to adapt to significantly different structural re-arrangements and accommodate structural changes in the catalytic domain whilst resisting the large torque generated by catalytic cycling. These results are important to understand the role the stators play in the rotary-ATPase mechanism. Proteins 2016; 84:1203-1212. © 2016 The Authors. Proteins: Structure, Function, and Bioinformatics Published by Wiley Periodicals, Inc.

摘要

旋转ATP酶参与众多生理过程,三种不同类型(F/A/V-ATP酶)具有共同的功能特性和结构特征。其基本机制涉及两个马达的反向旋转,一个是可溶性ATP水解/合成结构域,另一个是通过中心转子轴和定子复合体连接的膜嵌入离子泵。在A/V-ATP酶家族中,EG定子的构象灵活性已被证明可适应催化循环,并且被认为对功能很重要。对于A-ATP酶,已报道了三种EG结构,被认为代表旋转催化不同阶段定子的构象状态。在此,我们使用长时间、详细的原子模拟表明,这些结构是通过热涨落探索到的构象异构体,但并不代表溶液中EG定子的高丰度状态。我们表明,卷曲螺旋尾结构域具有较高的持久长度(约100 nm),但通过存在两个铰链区仍保留适应不同构象状态的能力。此外,除了催化结构域的核苷酸占据情况外,相关V-ATP酶的定子网络还被认为可适应套环区域中的亚基相互作用。此处报道的分子动力学模拟强化了这一观察结果,表明EG定子具有足够的灵活性以适应显著不同的结构重排,并在抵抗催化循环产生的大扭矩的同时适应催化结构域的结构变化。这些结果对于理解定子在旋转ATP酶机制中所起的作用很重要。《蛋白质》2016年;84:1203 - 1212。© 2016作者。《蛋白质:结构、功能与生物信息学》由威利期刊公司出版

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a6/4988496/1c4e863dc398/PROT-84-1203-g001.jpg

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