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MmpL3 蛋白中抑制剂结合和偶联运动的破坏:揭示海藻糖单胞壁酸转运的机制。

Inhibitor binding and disruption of coupled motions in MmpL3 protein: Unraveling the mechanism of trehalose monomycolate transport.

机构信息

Centre for Artificial Intelligence Driven Drug Discovery, Faculty of Applied Sciences, Macao Polytechnic University, Macao, China.

出版信息

Protein Sci. 2024 Oct;33(10):e5166. doi: 10.1002/pro.5166.

Abstract

Mycobacterial membrane protein Large 3 (MmpL3) of Mycobacterium tuberculosis (Mtb) is crucial for the translocation of trehalose monomycolate (TMM) across the inner bacterial cell membrane, making it a promising target for anti-tuberculosis (TB) drug development. While several structural, microbiological, and in vitro studies have provided significant insights, the precise mechanisms underlying TMM transport by MmpL3 and its inhibition remain incompletely understood at the atomic level. In this study, molecular dynamic (MD) simulations for the apo form and seven inhibitor-bound forms of Mtb MmpL3 were carried out to obtain a thorough comprehension of the protein's dynamics and function. MD simulations revealed that the seven inhibitors in this work stably bind to the central channel of the transmembrane domain and primarily forming hydrogen bonds with ASP251, ASP640, or both residues. Through dynamical cross-correlation matrix and principal component analysis analyses, several types of coupled motions between different domains were observed in the apo state, and distinct conformational states were identified using Markov state model analysis. These coupled motions and varied conformational states likely contribute to the transport of TMM. However, simulations of inhibitor-bound MmpL3 showed an enlargement of the proton channel, potentially disrupting coupled motions. This indicates that inhibitors may impair MmpL3's transport function by directly blocking the proton channel, thereby hindering coordinated domain movements and indirectly affecting TMM translocation.

摘要

结核分枝杆菌(Mycobacterium tuberculosis,Mtb)的分枝杆菌膜蛋白 Large 3(MmpL3)对于海藻糖单没食子酸酯(trehalose monomycolate,TMM)穿过细菌内膜的转运至关重要,使其成为抗结核(tuberculosis,TB)药物开发的有希望的靶标。虽然一些结构、微生物学和体外研究提供了重要的见解,但 MmpL3 转运 TMM 的精确机制及其抑制作用在原子水平上仍不完全了解。在这项研究中,对 Mtb MmpL3 的 apo 形式和七种抑制剂结合形式进行了分子动力学(molecular dynamic,MD)模拟,以全面理解该蛋白的动力学和功能。MD 模拟表明,本工作中的七种抑制剂稳定地结合在跨膜域的中央通道中,主要与 ASP251、ASP640 或这两个残基形成氢键。通过动态互相关矩阵和主成分分析分析,在 apo 状态下观察到不同结构域之间存在几种类型的耦合运动,并使用马尔可夫状态模型分析确定了不同的构象状态。这些耦合运动和不同的构象状态可能有助于 TMM 的转运。然而,抑制剂结合的 MmpL3 的模拟显示质子通道扩大,可能破坏了耦合运动。这表明抑制剂可能通过直接阻断质子通道来损害 MmpL3 的转运功能,从而阻碍协调的结构域运动,并间接影响 TMM 的转运。

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