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本文引用的文献

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Determination of the subunit stoichiometry of an inwardly rectifying potassium channel.内向整流钾通道亚基化学计量的测定
Neuron. 1995 Dec;15(6):1441-7. doi: 10.1016/0896-6273(95)90021-7.
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Potassium channel assembly from concatenated subunits: effects of proline substitutions in S4 segments.
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Inhibitory interactions between two inward rectifier K+ channel subunits mediated by the transmembrane domains.由跨膜结构域介导的两个内向整流钾通道亚基之间的抑制性相互作用。
J Biol Chem. 1996 Mar 8;271(10):5866-70. doi: 10.1074/jbc.271.10.5866.
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Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel.大鼠G蛋白偶联毒蕈碱钾通道的一级结构与功能表达
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Molecular cloning, functional expression and localization of an inward rectifier potassium channel in the mouse brain.小鼠脑中内向整流钾通道的分子克隆、功能表达及定位
FEBS Lett. 1993 Dec 28;336(3):375-80. doi: 10.1016/0014-5793(93)80840-q.
6
Atrial G protein-activated K+ channel: expression cloning and molecular properties.心房G蛋白激活的钾通道:表达克隆与分子特性
Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):10235-9. doi: 10.1073/pnas.90.21.10235.
7
The intrinsic gating of inward rectifier K+ channels expressed from the murine IRK1 gene depends on voltage, K+ and Mg2+.从小鼠IRK1基因表达的内向整流钾通道的内在门控取决于电压、钾离子和镁离子。
J Physiol. 1994 Feb 15;475(1):1-7. doi: 10.1113/jphysiol.1994.sp020044.
8
Gating of inwardly rectifying K+ channels localized to a single negatively charged residue.内向整流钾通道的门控定位在单个带负电荷的残基上。
Nature. 1994 Sep 15;371(6494):246-9. doi: 10.1038/371246a0.
9
Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification.细胞质多胺对钾通道的阻断作为内向整流的机制。
Nature. 1994 Nov 24;372(6504):366-9. doi: 10.1038/372366a0.
10
Cloning provides evidence for a family of inward rectifier and G-protein coupled K+ channels in the brain.克隆技术为大脑中内向整流钾通道和G蛋白偶联钾通道家族提供了证据。
FEBS Lett. 1994 Oct 10;353(1):37-42. doi: 10.1016/0014-5793(94)01007-2.

新型异源内向整流钾通道揭示的亚基位置效应

Subunit positional effects revealed by novel heteromeric inwardly rectifying K+ channels.

作者信息

Pessia M, Tucker S J, Lee K, Bond C T, Adelman J P

机构信息

Vollum Institute, Oregon Health Sciences University, Portland, OR 97201, USA.

出版信息

EMBO J. 1996 Jun 17;15(12):2980-7.

PMID:8670799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC450239/
Abstract

Kir 4.1 is an inward rectifier potassium channel subunit isolated from rat brain which forms homomeric channels when expressed in Xenopus oocytes; Kir 5.1 is a structurally related subunit which does not. Co-injection of mRNAs encoding Kir 4.1 and Kir 5.1 resulted in potassium currents that (i) were much larger than those seen from expression of Kir 4.1 alone, (ii) increased rather than decreased during several seconds at strongly negative potentials and (iii) had an underlying unitary conductance of 43 pS rather than the 12 pS seen with Kir 4.1 alone. In contrast, the properties of Kir 1.1, 2.1, 2.3, 3.1, 3.2 or 3.4 were not altered by coexpression with Kir 5.1. Expression of a concatenated cDNA encoding two or four linked subunits produced currents with the properties of co-expressed Kir 4.1 and Kir 5.1 when the subunits were connected 4-5 or 4-5-4-5, but not when they were connected 4-4-5-5. The results indicate that Kir 5.1 associates specifically with Kir 4.1 to form heteromeric channels, and suggest that they do so normally in the subunit order 4-5-4-5. Further, the relative order of subunits within the channel contributes to their functional properties.

摘要

Kir 4.1是从大鼠脑中分离出的内向整流钾通道亚基,当在非洲爪蟾卵母细胞中表达时可形成同聚体通道;Kir 5.1是一种结构相关的亚基,但不能形成同聚体通道。共注射编码Kir 4.1和Kir 5.1的mRNA可产生钾电流,其具有以下特点:(i)比单独表达Kir 4.1时观察到的电流大得多;(ii)在强负电位下持续数秒期间电流增加而非减少;(iii)潜在的单位电导为43 pS,而非单独表达Kir 4.1时的12 pS。相反,Kir 1.1、2.1、2.3、3.1、3.2或3.4与Kir 5.1共表达时其特性未发生改变。当编码两个或四个相连亚基的串联cDNA以4-5或4-5-4-5的顺序连接亚基时,表达产生的电流具有共表达Kir 4.1和Kir 5.1的特性,但以4-4-5-5的顺序连接时则不然。结果表明,Kir 5.1特异性地与Kir 4.1结合形成异聚体通道,并提示它们通常以4-5-4-5的亚基顺序结合。此外,通道内亚基的相对顺序有助于其功能特性。