Graduate Program in Biophysics, University of Wisconsin, Madison, WI.
Department of Neuroscience, University of Wisconsin, Madison, WI.
J Gen Physiol. 2019 Oct 7;151(10):1163-1172. doi: 10.1085/jgp.201912372. Epub 2019 Aug 20.
Key advances in single particle cryo-EM methods in the past decade have ushered in a resolution revolution in modern biology. The structures of many ion channels and transporters that were previously recalcitrant to crystallography have now been solved. Yet, despite having atomistic models of many complexes, some in multiple conformations, it has been challenging to glean mechanistic insight from these structures. To some extent this reflects our inability to unambiguously assign a given structure to a particular physiological state. One approach that may allow us to bridge this gap between structure and function is voltage clamp fluorometry (VCF). Using this technique, dynamic conformational changes can be measured while simultaneously monitoring the functional state of the channel or transporter. Many of the important papers that have used VCF to probe the gating mechanisms of channels and transporters have been published in the In this review, we provide an overview of the development of VCF and discuss some of the key problems that have been addressed using this approach. We end with a brief discussion of the outlook for this technique in the era of high-resolution structures.
过去十年中,单颗粒冷冻电子显微镜方法的重大进展引领了现代生物学的分辨率革命。许多先前对晶体学具有抗性的离子通道和转运蛋白的结构现已得到解决。然而,尽管已经有许多复合物的原子模型,其中一些处于多种构象,但是从这些结构中得出机械洞察力一直具有挑战性。在某种程度上,这反映了我们无法将给定的结构明确分配给特定的生理状态。一种可能使我们能够弥合结构和功能之间差距的方法是电压钳荧光法(VCF)。使用该技术,可以在同时监测通道或转运蛋白的功能状态的情况下测量动态构象变化。许多使用 VCF 来探究通道和转运蛋白的门控机制的重要论文已发表在《FEBS Journal》上。在本文综述中,我们概述了 VCF 的发展,并讨论了使用该方法解决的一些关键问题。最后,我们简要讨论了在高分辨率结构时代该技术的前景。