Rotation Mechanism of Molecular Motor V-ATPase Studied by Multiscale Molecular Dynamics Simulation

Overview

Journal Biophys J

Publisher Cell Press

Specialty Biophysics

Date 2017 Mar 16

PMID 28297650

Citations 7

Authors

Yuta Isaka

Toru Ekimoto

Yuichi Kokabu

Ichiro Yamato

Takeshi Murata

Mitsunori Ikeguchi

Affiliations

Soon will be listed here.

Abstract

Enterococcus hirae V-ATPase is a molecular motor composed of the AB hexamer ring and the central stalk. In association with ATP hydrolysis, three catalytic AB pairs in the AB ring undergo conformational changes, which lead to a 120° rotation of the central stalk. To understand how the conformational changes of three catalytic pairs induce the 120° rotation of the central stalk, we performed multiscale molecular dynamics (MD) simulations in which coarse-grained and all-atom MD simulations were combined using a fluctuation matching methodology. During the rotation, a catalytic AB pair spontaneously adopted an intermediate conformation, which was not included in the initial inputs of the simulations and was essentially close to the "bindable-like" structure observed in a recently solved crystal structure. Furthermore, the creation of a space between the bindable-like and tight pairs was required for the central stalk to rotate without steric hindrance. These cooperative rearrangements of the three catalytic pairs are crucial for the rotation of the central stalk.

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