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利用半胱氨酸残基的化学修饰来探究 Orai 通道的渗透性和门控性。

Interrogating permeation and gating of Orai channels using chemical modification of cysteine residues.

机构信息

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.

出版信息

Methods Enzymol. 2021;652:213-239. doi: 10.1016/bs.mie.2021.02.012. Epub 2021 Apr 5.

DOI:10.1016/bs.mie.2021.02.012
PMID:34059283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11927100/
Abstract

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.

摘要

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。

相似文献

1
Interrogating permeation and gating of Orai channels using chemical modification of cysteine residues.利用半胱氨酸残基的化学修饰来探究 Orai 通道的渗透性和门控性。
Methods Enzymol. 2021;652:213-239. doi: 10.1016/bs.mie.2021.02.012. Epub 2021 Apr 5.
2
Pore properties of Orai1 calcium channel dimers and their activation by the STIM1 ER calcium sensor.Orai1 钙通道二聚体的孔特性及其被 STIM1 ER 钙传感器激活。
J Biol Chem. 2018 Aug 17;293(33):12962-12974. doi: 10.1074/jbc.RA118.003424. Epub 2018 Jun 28.
3
CRAC channel opening is determined by a series of Orai1 gating checkpoints in the transmembrane and cytosolic regions.CRAC 通道的开启由跨膜区和胞质区一系列 Orai1 门控检查点决定。
J Biol Chem. 2021 Jan-Jun;296:100224. doi: 10.1074/jbc.RA120.015548. Epub 2020 Dec 29.
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Mapping the functional anatomy of Orai1 transmembrane domains for CRAC channel gating.绘制 Orai1 跨膜结构域功能解剖图以研究 CRAC 通道门控。
Proc Natl Acad Sci U S A. 2018 May 29;115(22):E5193-E5202. doi: 10.1073/pnas.1718373115. Epub 2018 May 14.
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Authentic CRAC channel activity requires STIM1 and the conserved portion of the Orai N terminus.真正的 CRAC 通道活性需要 STIM1 和 Orai N 端保守部分。
J Biol Chem. 2018 Jan 26;293(4):1259-1270. doi: 10.1074/jbc.M117.812206. Epub 2017 Dec 13.
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The basic residues in the Orai1 channel inner pore promote opening of the outer hydrophobic gate.Orai1 通道内孔中的基本残基促进了外疏水门的开启。
J Gen Physiol. 2020 Jan 6;152(1). doi: 10.1085/jgp.201912397.
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Gated regulation of CRAC channel ion selectivity by STIM1.STIM1 对 CRAC 通道离子选择性的门控调节。
Nature. 2012 Jan 25;482(7384):241-5. doi: 10.1038/nature10752.
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Orai1 mutations alter ion permeation and Ca2+-dependent fast inactivation of CRAC channels: evidence for coupling of permeation and gating.Orai1突变改变了CRAC通道的离子通透和Ca2+依赖性快速失活:通透与门控偶联的证据。
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ORAI1 channel gating and selectivity is differentially altered by natural mutations in the first or third transmembrane domain.ORAI1 通道门控和选择性通过第一或第三跨膜域中的天然突变而不同地改变。
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Twisting gating residues in the Orai pore.Orai孔道中扭转的门控残基。
Cell Calcium. 2021 Jan;93:102323. doi: 10.1016/j.ceca.2020.102323. Epub 2020 Dec 2.

本文引用的文献

1
Cryo-EM structure of the calcium release-activated calcium channel Orai in an open conformation.冷冻电镜结构解析钙释放激活钙通道 Orai 处于开放构象。
Elife. 2020 Nov 30;9:e62772. doi: 10.7554/eLife.62772.
2
A sulfur-aromatic gate latch is essential for opening of the Orai1 channel pore.硫芳族门闩对于 Orai1 通道孔的开启是必不可少的。
Elife. 2020 Oct 30;9:e60751. doi: 10.7554/eLife.60751.
3
The basic residues in the Orai1 channel inner pore promote opening of the outer hydrophobic gate.Orai1 通道内孔中的基本残基促进了外疏水门的开启。
J Gen Physiol. 2020 Jan 6;152(1). doi: 10.1085/jgp.201912397.
4
Molecular basis of allosteric Orai1 channel activation by STIM1.STIM1 对 Orai1 通道变构激活的分子基础。
J Physiol. 2020 May;598(9):1707-1723. doi: 10.1113/JP276550. Epub 2019 May 1.
5
Mapping the functional anatomy of Orai1 transmembrane domains for CRAC channel gating.绘制 Orai1 跨膜结构域功能解剖图以研究 CRAC 通道门控。
Proc Natl Acad Sci U S A. 2018 May 29;115(22):E5193-E5202. doi: 10.1073/pnas.1718373115. Epub 2018 May 14.
6
Transmembrane helix connectivity in Orai1 controls two gates for calcium-dependent transcription.Orai1 跨膜螺旋连接控制钙离子依赖型转录的两个门控。
Sci Signal. 2017 Nov 28;10(507):eaao0358. doi: 10.1126/scisignal.aao0358.
7
STIM1 activates CRAC channels through rotation of the pore helix to open a hydrophobic gate.STIM1 通过旋转孔螺旋激活 CRAC 通道,打开疏水性门。
Nat Commun. 2017 Feb 21;8:14512. doi: 10.1038/ncomms14512.
8
Pore opening mechanism of CRAC channels.CRAC通道的孔开放机制。
Cell Calcium. 2017 May;63:14-19. doi: 10.1016/j.ceca.2016.12.006. Epub 2016 Dec 23.
9
Analysis of the interactions of sulfur-containing amino acids in membrane proteins.膜蛋白中含硫氨基酸相互作用的分析
Protein Sci. 2016 Aug;25(8):1517-24. doi: 10.1002/pro.2955. Epub 2016 Jun 8.
10
Orai1 pore residues control CRAC channel inactivation independently of calmodulin.Orai1孔道残基独立于钙调蛋白控制CRAC通道失活。
J Gen Physiol. 2016 Feb;147(2):137-52. doi: 10.1085/jgp.201511437.