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本文引用的文献

1
Kinetics and thermodynamics of binding reactions as exemplified by anthrax toxin channel blockage with a cationic cyclodextrin derivative.结合反应的动力学和热力学:以阳离子环糊精衍生物阻断炭疽毒素通道为例。
Proc Natl Acad Sci U S A. 2012 Nov 6;109(45):18453-8. doi: 10.1073/pnas.1208771109. Epub 2012 Oct 24.
2
Analysis of transient receptor potential ankyrin 1 (TRPA1) in frogs and lizards illuminates both nociceptive heat and chemical sensitivities and coexpression with TRP vanilloid 1 (TRPV1) in ancestral vertebrates.分析瞬态受体电位锚蛋白 1(TRPA1)在青蛙和蜥蜴中的作用,揭示了其对伤害性热和化学物质的敏感性,以及在祖先脊椎动物中与 TRPV1 的共表达。
J Biol Chem. 2012 Aug 31;287(36):30743-54. doi: 10.1074/jbc.M112.362194. Epub 2012 Jul 12.
3
Selective disruption of high sensitivity heat activation but not capsaicin activation of TRPV1 channels by pore turret mutations.孔道转位突变选择性地破坏 TRPV1 通道对高灵敏度热激活而不是辣椒素激活的反应。
J Gen Physiol. 2012 Apr;139(4):273-83. doi: 10.1085/jgp.201110724. Epub 2012 Mar 12.
4
Quantifying and modeling the temperature-dependent gating of TRP channels.量化和建模温度依赖型 TRP 通道的门控。
Rev Physiol Biochem Pharmacol. 2012;162:91-119. doi: 10.1007/112_2011_5.
5
A thermodynamic framework for understanding temperature sensing by transient receptor potential (TRP) channels.理解瞬时受体电位 (TRP) 通道温度感应的热力学框架。
Proc Natl Acad Sci U S A. 2011 Dec 6;108(49):19492-7. doi: 10.1073/pnas.1117485108. Epub 2011 Nov 22.
6
Hysteresis of gating underlines sensitization of TRPV3 channels.门控滞后强调 TRPV3 通道的敏化作用。
J Gen Physiol. 2011 Nov;138(5):509-20. doi: 10.1085/jgp.201110689. Epub 2011 Oct 17.
7
Cytoplasmic ankyrin repeats of transient receptor potential A1 (TRPA1) dictate sensitivity to thermal and chemical stimuli.细胞质锚蛋白重复序列的瞬时受体电位 A1(TRPA1)决定了对热和化学刺激的敏感性。
Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):E1184-91. doi: 10.1073/pnas.1114124108. Epub 2011 Sep 19.
8
Modular thermal sensors in temperature-gated transient receptor potential (TRP) channels.温度门控瞬时受体电位(TRP)通道中的模块化热传感器。
Proc Natl Acad Sci U S A. 2011 Jul 5;108(27):11109-14. doi: 10.1073/pnas.1105196108. Epub 2011 Jun 20.
9
TRPM3 is a nociceptor channel involved in the detection of noxious heat.瞬时受体电位通道蛋白 3 是一种伤害感受器通道,参与伤害性热的检测。
Neuron. 2011 May 12;70(3):482-94. doi: 10.1016/j.neuron.2011.02.051.
10
Evolution of vertebrate transient receptor potential vanilloid 3 channels: opposite temperature sensitivity between mammals and western clawed frogs.脊椎动物瞬时受体电位香草素 3 通道的进化:哺乳动物和西方爪蟾之间的温度敏感性相反。
PLoS Genet. 2011 Apr;7(4):e1002041. doi: 10.1371/journal.pgen.1002041. Epub 2011 Apr 7.

变构偶联对热激活型瞬时受体电位通道的影响。

The role of allosteric coupling on thermal activation of thermo-TRP channels.

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.

出版信息

Biophys J. 2013 May 21;104(10):2160-9. doi: 10.1016/j.bpj.2013.03.055.

DOI:10.1016/j.bpj.2013.03.055
PMID:23708356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3660639/
Abstract

Thermo-transient receptor potential channels display outstanding temperature sensitivity and can be directly gated by low or high temperature, giving rise to cold- and heat-activated currents. These constitute the molecular basis for the detection of changes in ambient temperature by sensory neurons in animals. The mechanism that underlies the temperature sensitivity in thermo-transient receptor potential channels remains unknown, but has been associated with large changes in standard-state enthalpy (ΔH(o)) and entropy (ΔS(o)) upon channel gating. The magnitude, sign, and temperature dependence of ΔH(o) and ΔS(o), the last given by an associated change in heat capacity (ΔCp), can determine a channel's temperature sensitivity and whether it is activated by cooling, heating, or both, if ΔCp makes an important contribution. We show that in the presence of allosteric gating, other parameters, besides ΔH(o) and ΔS(o), including the gating equilibrium constant, the strength- and temperature dependence of the coupling between gating and the temperature-sensitive transitions, as well as the ΔH(o)/ΔS(o) ratio associated with them, can also determine a channel's temperature-dependent activity, and even give rise to channels that respond to both cooling and heating in a ΔCp-independent manner.

摘要

热激瞬时受体电位通道表现出卓越的温度敏感性,可直接被低温或高温门控,引发冷激活和热激活电流。这些构成了动物感觉神经元检测环境温度变化的分子基础。热激瞬时受体电位通道温度敏感性的机制尚不清楚,但与通道门控时标准态焓(ΔH(o))和熵(ΔS(o))的巨大变化有关。ΔH(o)和ΔS(o)的大小、符号和温度依赖性,以及由热容(ΔCp)相关变化给出的最后一个参数,可决定通道的温度敏感性,以及它是由冷却、加热还是两者共同激活,如果 ΔCp 有重要贡献的话。我们表明,在变构门控存在的情况下,除了 ΔH(o)和 ΔS(o)之外,其他参数,包括门控平衡常数、门控与温度敏感跃迁之间的耦合的强度和温度依赖性,以及与之相关的 ΔH(o)/ΔS(o)比值,也可以决定通道的温度依赖性活性,甚至产生以 ΔCp 独立的方式对冷却和加热均有响应的通道。