• 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

一种失活型电压敏感性钾离子通道的哺乳动物cDNA的特性分析。

Characterization of a mammalian cDNA for an inactivating voltage-sensitive K+ channel.

作者信息

Baldwin T J, Tsaur M L, Lopez G A, Jan Y N, Jan L Y

机构信息

Howard Hughes Medical Institute, University of California, San Francisco 94143-0724.

出版信息

Neuron. 1991 Sep;7(3):471-83. doi: 10.1016/0896-6273(91)90299-f.

DOI:10.1016/0896-6273(91)90299-f
PMID:1840649
Abstract

A cDNA clone encoding a K+ channel polypeptide with 72% amino acid sequence identity to Drosophila Shal was isolated from rat hippocampus. Functional expression of the cDNA in Xenopus oocytes generated 4-amino-pyridine-sensitive K+ channels displaying rapid inactivation kinetics. The fastest component of inactivation was slowed by the deletion of 3 basic residues in the amino-terminal region. Northern blots revealed that the mRNA encoding this K+ channel polypeptide was expressed at a similar level in the brain and in the heart. In situ hybridization revealed that the mRNA encoding this K+ channel appeared concentrated in the hippocampus, dentate gyrus, and habenular nucleus in the brain. Thus, this K+ channel polypeptide is likely to form some of the A-type K+ channels expressed in the mammalian nervous system and heart.

摘要

从大鼠海马体中分离出一个编码钾离子通道多肽的cDNA克隆,该多肽与果蝇Shal的氨基酸序列一致性为72%。该cDNA在非洲爪蟾卵母细胞中的功能性表达产生了对4-氨基吡啶敏感的钾离子通道,其显示出快速失活动力学。氨基末端区域3个碱性残基的缺失减缓了失活的最快组分。Northern印迹显示,编码该钾离子通道多肽的mRNA在脑和心脏中的表达水平相似。原位杂交显示,编码该钾离子通道的mRNA在脑中集中出现在海马体、齿状回和缰核中。因此,这种钾离子通道多肽可能构成哺乳动物神经系统和心脏中表达的一些A型钾离子通道。

相似文献

1
Characterization of a mammalian cDNA for an inactivating voltage-sensitive K+ channel.一种失活型电压敏感性钾离子通道的哺乳动物cDNA的特性分析。
Neuron. 1991 Sep;7(3):471-83. doi: 10.1016/0896-6273(91)90299-f.
2
A novel K+ channel with unique localizations in mammalian brain: molecular cloning and characterization.一种在哺乳动物大脑中具有独特定位的新型钾离子通道:分子克隆与特性分析。
Neuron. 1992 Mar;8(3):473-81. doi: 10.1016/0896-6273(92)90275-i.
3
Molecular cloning and functional expression of a potassium channel cDNA isolated from a rat cardiac library.从大鼠心脏文库中分离出的钾通道cDNA的分子克隆及功能表达
FEBS Lett. 1990 Jul 30;268(1):63-8. doi: 10.1016/0014-5793(90)80973-m.
4
Molecular cloning and functional characterization of a novel delayed rectifier potassium channel from channel catfish (Ictalurus punctatus): expression in taste buds.斑点叉尾鮰新型延迟整流钾通道的分子克隆与功能特性:味蕾中的表达
J Neurochem. 2001 Mar;76(5):1465-74. doi: 10.1046/j.1471-4159.2001.00137.x.
5
Molecular cloning and expression of an inwardly rectifying K(+) channel from bovine corneal endothelial cells.牛角膜内皮细胞内向整流钾通道的分子克隆与表达
Invest Ophthalmol Vis Sci. 2000 Sep;41(10):2936-44.
6
Cloning, expression and CNS distribution of Kv4.3, an A-type K+ channel alpha subunit.A 型钾离子通道α亚基Kv4.3的克隆、表达及在中枢神经系统中的分布
FEBS Lett. 1997 Jan 3;400(2):215-20. doi: 10.1016/s0014-5793(96)01388-9.
7
Sequence and functional expression in Xenopus oocytes of a human insulinoma and islet potassium channel.人胰岛素瘤及胰岛钾通道在非洲爪蟾卵母细胞中的序列及功能表达
Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):53-7. doi: 10.1073/pnas.88.1.53.
8
Cloning and functional expression of a novel cardiac two-pore background K+ channel (cTBAK-1).一种新型心脏双孔背景钾通道(cTBAK-1)的克隆与功能表达
Circ Res. 1998 Mar 9;82(4):513-8. doi: 10.1161/01.res.82.4.513.
9
Molecular cloning and functional expression of a novel potassium channel beta-subunit from human atrium.
FEBS Lett. 1995 Mar 13;361(1):13-6. doi: 10.1016/0014-5793(95)00120-x.
10
The voltage-dependent K+ channel (Kv1.5) cloned from rabbit heart and facilitation of inactivation of the delayed rectifier current by the rat beta subunit.从兔心脏克隆的电压依赖性钾通道(Kv1.5)以及大鼠β亚基对延迟整流电流失活的促进作用。
FEBS Lett. 1995 Sep 18;372(1):20-4. doi: 10.1016/0014-5793(95)00954-8.

引用本文的文献

1
The Voltage-Gated Potassium Channel (K4) Contributes to Active Hearing in .电压门控钾通道(K4)有助于[具体物种未给出]的主动听觉。
eNeuro. 2025 Jan 9;12(1). doi: 10.1523/ENEURO.0083-24.2024. Print 2025 Jan.
2
Flavonoids as Modulators of Potassium Channels.类黄酮作为钾通道调节剂。
Int J Mol Sci. 2023 Jan 9;24(2):1311. doi: 10.3390/ijms24021311.
3
Neuronal Roles of the Multifunctional Protein Dipeptidyl Peptidase-like 6 (DPP6).多功能蛋白二肽基肽酶样 6(DPP6)的神经元作用。
Int J Mol Sci. 2022 Aug 16;23(16):9184. doi: 10.3390/ijms23169184.
4
Potassium Channel Conductance Is Involved in Phenylephrine-Induced Spontaneous Firing of Serotonergic Neurons in the Dorsal Raphe Nucleus.钾通道电导参与去氧肾上腺素诱导的中缝背核5-羟色胺能神经元自发放电。
Front Cell Neurosci. 2022 Jun 6;16:891912. doi: 10.3389/fncel.2022.891912. eCollection 2022.
5
Activation and closed-state inactivation mechanisms of the human voltage-gated K4 channel complexes.人类电压门控 K4 通道复合物的激活和失活机制。
Mol Cell. 2022 Jul 7;82(13):2427-2442.e4. doi: 10.1016/j.molcel.2022.04.032. Epub 2022 May 20.
6
Variation of Two S3b Residues in K4.1-4.3 Channels Underlies Their Different Modulations by Spider Toxin κ-LhTx-1.K4.1 - 4.3通道中两个S3b残基的变异是蜘蛛毒素κ-LhTx-1对其产生不同调节作用的基础。
Front Pharmacol. 2021 Jun 10;12:692076. doi: 10.3389/fphar.2021.692076. eCollection 2021.
7
Impaired pattern separation in Tg2576 mice is associated with hyperexcitable dentate gyrus caused by Kv4.1 downregulation.Tg2576 小鼠的模式分离受损与 Kv4.1 下调引起的齿状回过度兴奋有关。
Mol Brain. 2021 Mar 30;14(1):62. doi: 10.1186/s13041-021-00774-x.
8
Kv4.1, a Key Ion Channel For Low Frequency Firing of Dentate Granule Cells, Is Crucial for Pattern Separation.Kv4.1,一种调节齿状回颗粒细胞低频放电的关键离子通道,对模式分离至关重要。
J Neurosci. 2020 Mar 11;40(11):2200-2214. doi: 10.1523/JNEUROSCI.1541-19.2020. Epub 2020 Feb 11.
9
Nociceptor Signalling through ion Channel Regulation via GPCRs.伤害感受器通过 G 蛋白偶联受体的离子通道调节进行信号传递。
Int J Mol Sci. 2019 May 20;20(10):2488. doi: 10.3390/ijms20102488.
10
A-Type K Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction.背根神经节神经元中的A型钾通道:多样性、功能及功能障碍
Front Mol Neurosci. 2018 Aug 6;11:253. doi: 10.3389/fnmol.2018.00253. eCollection 2018.