Suppr超能文献

加兰他敏阻断揭示的肌浆网钾通道的结构方面

Structural aspects of the sarcoplasmic reticulum K+ channel revealed by gallamine block.

作者信息

Gray M A, Tomlins B, Montgomery R A, Williams A J

机构信息

Department of Cardiac Medicine, University of London, United Kingdom.

出版信息

Biophys J. 1988 Aug;54(2):233-9. doi: 10.1016/S0006-3495(88)82952-7.

Abstract

We have studied single-channel conductance fluctuations of K+ channels present in the sarcoplasmic reticulum (SR) membrane systems of rabbit cardiac and skeletal muscle. K+ conductance through the channels is reversibly blocked by gallamine. Conductance block occurs only from the trans side of the channel and is resolved as a smooth reduction in the open state conductance. At a fixed K+ concentration, conduction decreases with increasing gallamine concentration and the data can be fitted to a single-site inhibition scheme. The degree of block seen at a constant gallamine concentration decreases as K+ concentration is increased, indicating competition between gallamine and K+. Gallamine block is voltage dependent, the degree of block increasing with increasing negative holding potential. Quantitative analysis of block yields a zero voltage dissociation constant of 55.3 +/- 16 microM and an effective valence of block of 0.93 +/- 0.12. We conclude that gallamine blocks by interacting with a site or sites located at an electrical distance 30-35% into the voltage drop from the trans side of the channel. This site must have a cross-sectional area of at least 1.2 nm2. The results of this study have been used to modify and extend our view of the structure of the channel's conduction pathway.

摘要

我们研究了兔心脏和骨骼肌肌浆网(SR)膜系统中存在的钾离子通道的单通道电导波动情况。通过这些通道的钾离子电导可被加拉明可逆性阻断。电导阻断仅从通道的胞外侧发生,且表现为开放状态电导的平稳降低。在固定的钾离子浓度下,随着加拉明浓度增加,传导性降低,并且数据可拟合为单位点抑制模式。在恒定的加拉明浓度下,随着钾离子浓度增加,观察到的阻断程度降低,表明加拉明与钾离子之间存在竞争。加拉明阻断具有电压依赖性,阻断程度随负性钳制电位增加而增加。对阻断的定量分析得出零电压解离常数为55.3±16微摩尔,有效阻断价为0.93±0.12。我们得出结论,加拉明通过与位于通道胞外侧电压降30 - 35%处的一个或多个位点相互作用而产生阻断。该位点的横截面积必须至少为1.2平方纳米。本研究结果已用于修正和扩展我们对通道传导途径结构的认识。

相似文献

1
Structural aspects of the sarcoplasmic reticulum K+ channel revealed by gallamine block.
Biophys J. 1988 Aug;54(2):233-9. doi: 10.1016/S0006-3495(88)82952-7.
2
The K+ channel of sarcoplasmic reticulum. A new look at Cs+ block.
Biophys J. 1985 Sep;48(3):477-84. doi: 10.1016/S0006-3495(85)83803-0.
4
Effects of phospholipid surface charge on ion conduction in the K+ channel of sarcoplasmic reticulum.
Biophys J. 1984 Jan;45(1):279-87. doi: 10.1016/S0006-3495(84)84154-5.

引用本文的文献

本文引用的文献

1
Blockage of squid axon potassium conductance by internal tetra-N-alkylammonium ions of various sizes.
Biophys J. 1981 May;34(2):271-91. doi: 10.1016/S0006-3495(81)84849-7.
2
Effect of pore structure on energy barriers and applied voltage profiles. II. Unsymmetrical channels.
Biophys J. 1984 Jun;45(6):1101-7. doi: 10.1016/s0006-3495(84)84258-7.
3
Effect of pore structure on energy barriers and applied voltage profiles. I. Symmetrical channels.
Biophys J. 1984 Jun;45(6):1091-100. doi: 10.1016/S0006-3495(84)84257-5.
4
Channel-mediated monovalent cation fluxes in isolated sarcoplasmic reticulum vesicles.
J Gen Physiol. 1984 Jun;83(6):819-39. doi: 10.1085/jgp.83.6.819.
5
Conduction and selectivity in potassium channels.
J Membr Biol. 1983;71(1-2):11-30. doi: 10.1007/BF01870671.
6
Electrostatic modeling of ion pores. Energy barriers and electric field profiles.
Biophys J. 1982 Aug;39(2):157-64. doi: 10.1016/S0006-3495(82)84503-7.
7
Coupling of water and ion fluxes in a K+-selective channel of sarcoplasmic reticulum.
Biophys J. 1982 Jun;38(3):227-30. doi: 10.1016/S0006-3495(82)84552-9.
8
Bis-quaternary ammonium blockers as structural probes of the sarcoplasmic reticulum K+ channel.
J Gen Physiol. 1982 May;79(5):869-91. doi: 10.1085/jgp.79.5.869.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验