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本文引用的文献

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ASIC3 channels in multimodal sensory perception.ASIC3 通道在多模态感觉感知中的作用。
ACS Chem Neurosci. 2011 Jan 19;2(1):26-37. doi: 10.1021/cn100094b. Epub 2010 Nov 12.
2
A heteromeric Texas coral snake toxin targets acid-sensing ion channels to produce pain.一种异源德州珊瑚蛇毒素靶向酸感应离子通道产生疼痛。
Nature. 2011 Nov 16;479(7373):410-4. doi: 10.1038/nature10607.
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Neuroscience: chemical ecology of pain.神经科学:疼痛的化学生态学
Nature. 2011 Nov 16;479(7373):306-7. doi: 10.1038/479306a.
4
Nonproton ligand sensing domain is required for paradoxical stimulation of acid-sensing ion channel 3 (ASIC3) channels by amiloride.非质子配体感应结构域是阿米洛利对酸敏感离子通道 3 (ASIC3) 通道反常刺激所必需的。
J Biol Chem. 2011 Dec 9;286(49):42635-42646. doi: 10.1074/jbc.M111.289058. Epub 2011 Oct 13.
5
Chemical and genetic engineering of selective ion channel-ligand interactions.选择性离子通道-配体相互作用的化学和遗传工程。
Science. 2011 Sep 2;333(6047):1292-6. doi: 10.1126/science.1206606.
6
Estimating the pKa values of basic and acidic side chains in ion channels using electrophysiological recordings: a robust approach to an elusive problem.使用电生理记录估算离子通道中碱性和酸性侧链的 pKa 值:解决难题的稳健方法。
Proteins. 2011 Dec;79(12):3485-93. doi: 10.1002/prot.23087. Epub 2011 Jul 8.
7
Zinc alleviates pain through high-affinity binding to the NMDA receptor NR2A subunit.锌通过与 NMDA 受体 NR2A 亚基的高亲和力结合来缓解疼痛。
Nat Neurosci. 2011 Jul 3;14(8):1017-22. doi: 10.1038/nn.2844.
8
Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gating.半胱氨酸扫描诱变(Glu52-Gly96 残基)对人 P2X1 受体的 ATP 作用:结合激动剂和通道门控的映射。
J Biol Chem. 2011 Aug 19;286(33):29207-29217. doi: 10.1074/jbc.M111.260364. Epub 2011 Jun 20.
9
Tunable pKa values and the basis of opposite charge selectivities in nicotinic-type receptors.可调节的 pKa 值和烟碱型受体中相反电荷选择性的基础。
Nature. 2011 May 22;474(7352):526-30. doi: 10.1038/nature10015.
10
Atomic level characterization of the nonproton ligand-sensing domain of ASIC3 channels.ASIC3 通道中非质子配体感应结构域的原子水平表征。
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新兴的离子通道结构与功能探测方法。

Emerging approaches to probing ion channel structure and function.

机构信息

Neuroscience Division, Department of Biochemistry and Molecular Cell Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

出版信息

Neurosci Bull. 2012 Aug;28(4):351-74. doi: 10.1007/s12264-012-1248-0.

DOI:10.1007/s12264-012-1248-0
PMID:22833035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5561889/
Abstract

Ion channels, as membrane proteins, are the sensors of the cell. They act as the first line of communication with the world beyond the plasma membrane and transduce changes in the external and internal environments into unique electrical signals to shape the responses of excitable cells. Because of their importance in cellular communication, ion channels have been intensively studied at the structural and functional levels. Here, we summarize the diverse approaches, including molecular and cellular, chemical, optical, biophysical, and computational, used to probe the structural and functional rearrangements that occur during channel activation (or sensitization), inactivation (or desensitization), and various forms of modulation. The emerging insights into the structure and function of ion channels by multidisciplinary approaches allow the development of new pharmacotherapies as well as new tools useful in controlling cellular activity.

摘要

离子通道作为膜蛋白,是细胞的感应器。它们充当着与质膜之外世界进行交流的第一道防线,将外部和内部环境的变化转化为独特的电信号,从而塑造可兴奋细胞的反应。由于其在细胞通讯中的重要性,离子通道在结构和功能层面上得到了深入研究。在这里,我们总结了多种方法,包括分子和细胞、化学、光学、生物物理和计算方法,用于探测通道激活(或敏化)、失活(或脱敏)以及各种形式的调节过程中发生的结构和功能重排。多学科方法对离子通道结构和功能的新见解,使得新的药物治疗方法以及控制细胞活动的新工具得以发展。