Department of Pharmacology, Northwestern University, Feinberg School of Medicine, Chicago, IL, United States.
Department of Pharmacology, Northwestern University, Feinberg School of Medicine, Chicago, IL, United States.
Methods Enzymol. 2021;652:213-239. doi: 10.1016/bs.mie.2021.02.012. Epub 2021 Apr 5.
Chemical modification of ion channels using the substituted cysteine accessibility method has a rich and successful history in elucidating the structural basis of ion channel function. In this approach, cysteine residues are introduced in regions of interest into the protein and their accessibility to water soluble thiol-reactive reagents is determined by monitoring ion channel activity. Because a wide range of these reagents are available with differing size, charge, and membrane solubility, the physio-chemical environment of the introduced cysteine residue and therefore the protein domain of interest can be probed with great precision. The approach has been widely employed for determining the secondary structure of specific ion channel domains, the location and nature of the channel gate, and the conformational rearrangements in the channel pore that underlie the opening/closing of the pore. In this chapter, we describe the use of these and related approaches to probe the functional architecture and gating of store-operated Orai1 channels.
使用取代半胱氨酸可及性方法对离子通道进行化学修饰,在阐明离子通道功能的结构基础方面有着丰富而成功的历史。在这种方法中,将半胱氨酸残基引入蛋白质的感兴趣区域,并通过监测离子通道活性来确定其对半水溶性巯基反应性试剂的可及性。由于有广泛的具有不同大小、电荷和膜溶性的这些试剂可用,因此可以非常精确地探测引入的半胱氨酸残基的生理化学环境,即感兴趣的蛋白质结构域。该方法已广泛用于确定特定离子通道结构域的二级结构、通道门的位置和性质,以及构成孔道开闭基础的通道孔中的构象重排。在本章中,我们描述了这些方法及相关方法在探测储存操作的 Orai1 通道的功能结构和门控中的应用。