Analysis of the Interactions between Arp2/3 Complex and an Inhibitor Arpin by Molecular Dynamics Simulation


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The Arp2/3 complex is one of the main regulators of the actin cytoskeleton and a basic molecular machine that nucleates the branched actin filaments. In this work, we studied the interaction of the Arp2/3 complex with its inhibitor, arpin, and revealed the amino-acid residues that are responsible for complex formation. The free-energy calculation for arpin binding to the Arp2/3 complex was performed using umbrella sampling. It has been shown that the dissociation constant of the Arp2/3–arpin complex is higher on average than that of Arp2/3 complexes with other inhibitors. Two arpin binding sites with different affinities were identified on the surface of the Arp2/3 complex. The mechanism of the inhibition of the Arp2/3 complex by arpin is discussed.

作者简介

A. Popinako

Bach Institute of Biochemistry, Research Center of Biotechnology

Email: sokolova@mail.bio.msu.ru
俄罗斯联邦, Moscow, 119071

M. Antonov

Ammosov Northeastern Federal University

Email: sokolova@mail.bio.msu.ru
俄罗斯联邦, Yakutsk, Republic of Sakha (Yakutia), 677980

A. Chemeris

Moscow State University

Email: sokolova@mail.bio.msu.ru
俄罗斯联邦, Moscow, 119991

K. Shaitan

Moscow State University; Semenov Institute of Chemical Physics

Email: sokolova@mail.bio.msu.ru
俄罗斯联邦, Moscow, 119991; Moscow, 119991

O. Sokolova

Moscow State University

编辑信件的主要联系方式.
Email: sokolova@mail.bio.msu.ru
俄罗斯联邦, Moscow, 119991

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