• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于准生理离子条件下的整流特性对双孔结构域钾通道进行分类。

Classification of 2-pore domain potassium channels based on rectification under quasi-physiological ionic conditions.

作者信息

Chen Haijun, Zuo Dongchuan, Zhang Jianing, Zhou Min, Ma Liqun

机构信息

a Department of Biological Sciences ; University at Albany; State University of New York ; Albany , NY USA.

出版信息

Channels (Austin). 2014;8(6):503-8. doi: 10.4161/19336950.2014.973779.

DOI:10.4161/19336950.2014.973779
PMID:25616686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5290589/
Abstract

It is generally expected that 2-pore domain K(+) (K2P) channels are open or outward rectifiers in asymmetric physiological K(+) gradients, following the Goldman-Hodgkin-Katz (GHK) current equation. Although cloned K2P channels have been extensively studied, their current-voltage (I-V) relationships are not precisely characterized and previous definitions are contradictory. Here we study all the functional channels from 6 mammalian K2P subfamilies in transfected Chinese hamster ovary cells with patch-clamp technique, and examine whether their I-V relationships are described by the GHK current equation. K2P channels display 2 distinct types of I-V curves in asymmetric physiological K(+) gradients. Two K2P isoforms in the TWIK subfamily conduct large inward K(+) currents and have a nearly linear I-V curve. Ten isoforms from 5 other K2P subfamilies conduct small inward K(+) currents and exhibit open rectification, but fits with the GHK current equation cannot precisely reveal the differences in rectification among K2P channels. The Rectification Index, a ratio of limiting I-V slopes for outward and inward currents, is used to quantitatively describe open rectification of each K2P isoform, which is previously qualitatively defined as strong or weak open rectification. These results systematically and precisely classify K2P channels and suggest that TWIK K(+) channels have a unique feature in regulating cellular function.

摘要

一般认为,在不对称的生理钾离子梯度中,双孔结构域钾离子(K2P)通道是开放的或外向整流的,符合戈德曼-霍奇金-卡茨(GHK)电流方程。尽管克隆的K2P通道已得到广泛研究,但其电流-电压(I-V)关系并未得到精确表征,且先前的定义相互矛盾。在这里,我们用膜片钳技术研究了转染的中国仓鼠卵巢细胞中6个哺乳动物K2P亚家族的所有功能通道,并检验它们的I-V关系是否能用GHK电流方程来描述。在不对称的生理钾离子梯度中,K2P通道呈现出两种不同类型的I-V曲线。TWIK亚家族中的两种K2P亚型传导大量内向钾离子电流,且具有近乎线性的I-V曲线。来自其他5个K2P亚家族的10种亚型传导小的内向钾离子电流,并表现出开放整流,但与GHK电流方程的拟合并不能精确揭示K2P通道之间整流的差异。整流指数是外向电流与内向电流的极限I-V斜率之比,用于定量描述每种K2P亚型的开放整流,此前该整流被定性定义为强或弱开放整流。这些结果对K2P通道进行了系统而精确的分类,并表明TWIK钾离子通道在调节细胞功能方面具有独特的特征。

相似文献

1
Classification of 2-pore domain potassium channels based on rectification under quasi-physiological ionic conditions.基于准生理离子条件下的整流特性对双孔结构域钾通道进行分类。
Channels (Austin). 2014;8(6):503-8. doi: 10.4161/19336950.2014.973779.
2
Acid-sensitive TWIK and TASK two-pore domain potassium channels change ion selectivity and become permeable to sodium in extracellular acidification.酸敏感的 TWIK 和 TASK 双孔钾通道在细胞外酸化时改变离子选择性并对钠离子通透。
J Biol Chem. 2012 Oct 26;287(44):37145-53. doi: 10.1074/jbc.M112.398164. Epub 2012 Sep 4.
3
Na(+)-induced inward rectification in the two-pore domain K(+) channel, TASK-2.两孔结构域钾通道TASK-2中的钠离子诱导内向整流
Am J Physiol Renal Physiol. 2005 Jan;288(1):F162-9. doi: 10.1152/ajprenal.00248.2004. Epub 2004 Aug 24.
4
Regulation of two-pore-domain (K2P) potassium leak channels by the tyrosine kinase inhibitor genistein.酪氨酸激酶抑制剂金雀异黄素对双孔结构域(K2P)钾离子渗漏通道的调控作用
Br J Pharmacol. 2008 Aug;154(8):1680-90. doi: 10.1038/bjp.2008.213. Epub 2008 Jun 2.
5
Vernakalant activates human cardiac K(2P)17.1 background K(+) channels.维纳卡兰可激活人类心脏K(2P)17.1背景钾通道。
Biochem Biophys Res Commun. 2014 Aug 29;451(3):415-20. doi: 10.1016/j.bbrc.2014.07.133. Epub 2014 Aug 7.
6
Class I antiarrhythmic drugs inhibit human cardiac two-pore-domain K(+) (K2 ₂p) channels.I 类抗心律失常药物抑制人心肌双孔域钾 (K₂p) 通道。
Eur J Pharmacol. 2013 Dec 5;721(1-3):237-48. doi: 10.1016/j.ejphar.2013.09.029. Epub 2013 Sep 23.
7
Inhibition of cardiac two-pore-domain K+ (K2P) channels by the antiarrhythmic drug vernakalant--comparison with flecainide.抗心律失常药物维纳卡兰对心脏双孔结构域钾离子(K2P)通道的抑制作用——与氟卡尼的比较。
Eur J Pharmacol. 2014 Feb 5;724:51-7. doi: 10.1016/j.ejphar.2013.12.030. Epub 2013 Dec 27.
8
Selectivity filter instability dominates the low intrinsic activity of the TWIK-1 K2P K channel.选择性过滤器的不稳定性主导了TWIK-1 K2P钾通道的低固有活性。
J Biol Chem. 2020 Jan 10;295(2):610-618. doi: 10.1074/jbc.RA119.010612. Epub 2019 Dec 5.
9
Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels.卡维地洛靶向人 K2P3.1(TASK1)钾离子泄漏通道。
Br J Pharmacol. 2011 Jul;163(5):1099-110. doi: 10.1111/j.1476-5381.2011.01319.x.
10
Novel electrophysiological properties of dronedarone: inhibition of human cardiac two-pore-domain potassium (K2P) channels.新型电生理特性的决奈达隆:抑制人心双孔钾(K2P)通道。
Naunyn Schmiedebergs Arch Pharmacol. 2012 Oct;385(10):1003-16. doi: 10.1007/s00210-012-0780-9. Epub 2012 Jul 13.

引用本文的文献

1
Unraveling the Molecular Reason of Opposing Effects of α-Mangostin and Norfluoxetine on TREK-2 at the Same Binding Site.揭示α-山竹黄酮和去甲氟西汀在同一结合位点对TREK-2产生相反作用的分子机制。
ChemMedChem. 2024 Dec 2;19(23):e202400409. doi: 10.1002/cmdc.202400409. Epub 2024 Oct 21.
2
Non-trivial dynamics in a model of glial membrane voltage driven by open potassium pores.由开放钾离子通道驱动的神经胶质细胞膜电压的重要动力学模型。
Biophys J. 2023 Apr 18;122(8):1470-1490. doi: 10.1016/j.bpj.2023.03.013. Epub 2023 Mar 13.

本文引用的文献

1
Acid-sensitive TWIK and TASK two-pore domain potassium channels change ion selectivity and become permeable to sodium in extracellular acidification.酸敏感的 TWIK 和 TASK 双孔钾通道在细胞外酸化时改变离子选择性并对钠离子通透。
J Biol Chem. 2012 Oct 26;287(44):37145-53. doi: 10.1074/jbc.M112.398164. Epub 2012 Sep 4.
2
Crystal structure of the human K2P TRAAK, a lipid- and mechano-sensitive K+ ion channel.人类 K2P TRAAK 通道的晶体结构,一种脂质和机械敏感性钾离子通道。
Science. 2012 Jan 27;335(6067):436-41. doi: 10.1126/science.1213808.
3
Crystal structure of the human two-pore domain potassium channel K2P1.人双孔域钾通道 K2P1 的晶体结构。
Science. 2012 Jan 27;335(6067):432-6. doi: 10.1126/science.1213274.
4
TWIK-1 two-pore domain potassium channels change ion selectivity and conduct inward leak sodium currents in hypokalemia.TWIK-1 双孔钾通道在低钾血症中改变离子选择性并传导内向渗漏钠电流。
Sci Signal. 2011 Jun 7;4(176):ra37. doi: 10.1126/scisignal.2001726.
5
Molecular background of leak K+ currents: two-pore domain potassium channels.漏钾电流的分子基础:双孔域钾通道。
Physiol Rev. 2010 Apr;90(2):559-605. doi: 10.1152/physrev.00029.2009.
6
Potassium channel silencing by constitutive endocytosis and intracellular sequestration.钾通道通过组成型内吞作用和细胞内隔离而失活。
J Biol Chem. 2010 Feb 12;285(7):4798-805. doi: 10.1074/jbc.M109.078535. Epub 2009 Dec 3.
7
Characterization of TWIK-2, a two-pore domain K+ channel, cloned from the rat middle cerebral artery.从大鼠大脑中动脉克隆的双孔结构域钾通道TWIK-2的特性分析
Exp Biol Med (Maywood). 2009 Dec;234(12):1493-502. doi: 10.3181/0903-RM-110.
8
POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES.膜的电位、阻抗和整流。
J Gen Physiol. 1943 Sep 20;27(1):37-60. doi: 10.1085/jgp.27.1.37.
9
TWIK-1 and TREK-1 are potassium channels contributing significantly to astrocyte passive conductance in rat hippocampal slices.TWIK-1和TREK-1是钾通道,对大鼠海马切片中星形胶质细胞的被动电导有显著贡献。
J Neurosci. 2009 Jul 1;29(26):8551-64. doi: 10.1523/JNEUROSCI.5784-08.2009.
10
Emerging roles for two-pore-domain potassium channels and their potential therapeutic impact.双孔结构域钾通道的新作用及其潜在治疗意义。
Trends Pharmacol Sci. 2008 Nov;29(11):566-75. doi: 10.1016/j.tips.2008.07.013. Epub 2008 Sep 25.