Morris Richard G
National Centre for Biological Sciences, Tata Institute for Fundamental Research, GKVK, Bangalore, India.
Biophys J. 2017 Jan 10;112(1):3-9. doi: 10.1016/j.bpj.2016.12.009.
The question of how mechanically gated membrane channels open and close is notoriously difficult to address, especially if the protein structure is not available. This perspective highlights the relevance of micropipette-aspirated single-particle tracking-used to obtain a channel's diffusion coefficient, D, as a function of applied membrane tension, σ-as an indirect assay for determining functional behavior in mechanosensitive channels. While ensuring that the protein remains integral to the membrane, such methods can be used to identify not only the gating mechanism of a protein, but also associated physical moduli, such as torsional and dilational rigidity, which correspond to the protein's effective shape change. As an example, three distinct D-versus-σ "signatures" are calculated, corresponding to gating by dilation, gating by tilt, and gating by a combination of both dilation and tilt. Both advantages and disadvantages of the approach are discussed.
机械门控膜通道如何开启和关闭的问题 notoriously 难以解决,尤其是在蛋白质结构未知的情况下。本文观点强调了微量吸管抽吸单粒子追踪的相关性——用于获得通道扩散系数D作为施加膜张力σ的函数——作为一种间接测定机械敏感通道功能行为的方法。在确保蛋白质与膜保持完整的同时,此类方法不仅可用于识别蛋白质的门控机制,还可用于识别相关的物理模量,如扭转刚度和膨胀刚度,它们对应于蛋白质的有效形状变化。例如,计算了三种不同的D与σ“特征”,分别对应于由扩张引起的门控、由倾斜引起的门控以及由扩张和倾斜组合引起的门控。文中讨论了该方法的优缺点。 (注:“notoriously”此处暂保留英文未翻译,因为没有更合适的中文准确对应其在语境中的含义)