Department of Chemistry, University of Texas at Austin , Austin, Texas 78712, United States.
Institute for Computational Engineering and Sciences, University of Texas at Austin , Austin, Texas 78712, United States.
J Am Chem Soc. 2017 Oct 25;139(42):14837-14840. doi: 10.1021/jacs.7b07419. Epub 2017 Oct 12.
We report atomically detailed molecular dynamics simulations of the permeation of the lethal factor (LF) N-terminal segment through the anthrax channel. The N-terminal chain is unstructured and leads the permeation process for the LF protein. The simulations were conducted in explicit solvent with milestoning theory, making it possible to extract kinetic information from nanosecond to millisecond time scales. We illustrate that the initial event is strongly influenced by the protonation states of the permeating amino acids. While the N-terminal segment passes easily at high protonation state through the anthrax channel (and the ϕ clamp), the initial permeation represents a critical step, which can be irreversible and establishes a hook in the channel mouth.
我们报告了原子细节的分子动力学模拟穿透炭疽通道的致死因子 (LF) N 端片段。N 端链是无结构的,并为 LF 蛋白的渗透过程提供指导。模拟是在显式溶剂中进行的,里程碑理论使得能够从纳秒到毫秒时间尺度提取动力学信息。我们说明初始事件强烈受到渗透氨基酸的质子化状态的影响。虽然 N 端片段在高质子化状态下很容易通过炭疽通道(和 ϕ 夹),但初始渗透代表一个关键步骤,可能是不可逆的,并在通道口形成一个钩子。