Zheng Jie, Zagotta William N
Howard Hughes Medical Institute, Department of Physiology and Biophysics, University of Washington School of Medicine, Box 357290, Seattle, WA 98195, USA.
Sci STKE. 2003 Apr 1;2003(176):PL7. doi: 10.1126/stke.2003.176.pl7.
Conformational rearrangements are commonly observed in membrane proteins and constitute the molecular mechanisms through which they contribute to signal transduction. Information on structural changes in membrane proteins has mostly been inferred from functional studies. Recently, site-specific fluorescence recordings have made it possible to directly observe such molecular events in real time within the membrane environment. Here, we describe the patch-clamp fluorometry (PCF) technique that records simultaneously the local structural changes and the functional states of ion channels in isolated cell membranes. Combined with fluorescence resonance energy transfer (FRET), the technique should shed new light on ion channel activation, regulation, and interaction with other membrane proteins.
构象重排常见于膜蛋白中,是它们参与信号转导的分子机制。关于膜蛋白结构变化的信息大多是从功能研究中推断出来的。最近,位点特异性荧光记录使得在膜环境中实时直接观察此类分子事件成为可能。在这里,我们描述了膜片钳荧光测定法(PCF)技术,该技术可同时记录分离细胞膜中离子通道的局部结构变化和功能状态。结合荧光共振能量转移(FRET),该技术将为离子通道的激活、调节以及与其他膜蛋白的相互作用提供新的见解。