课题基金 / 基金详情

MOLECULAR PHYSIOLOGY OF CARDIAC POTASSIUM CHANNELS

MOLECULAR PHYSIOLOGY OF CARDIAC POTASSIUM CHANNELS
心脏钾通道的分子生理学
批准号:
6125770
负责人:
CAROL A VANDENBERG
金额:
$22.11万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-04-01 至 2001-11-30

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中文摘要
翻译
这个项目的目标是了解的分子基础
英文摘要
The goal of this project is an understanding of the molecular basis of the structure and function of inwardly rectifying potassium channels. These channels are central to the functioning of cardiac cells where they are involved in controlling the action potential waveform, duration, resting potential and controlling cell excitability. This proposal concentrates on the inward rectifier channels of the K1 class that show strong asymmetry in potassium conductance and are found prominently in heart and brain. The goal of this project is to use an integrated molecular, biophysical and biochemical approach to investigate a) the functional permeation, conduction and rectification properties of K1 channels, b) the channel polypeptide transmembrane topology, and c) the subunit composition and assembly of inward rectifier channels. The specific aims of the project are: Aim 1. The functional characteristics of the channels will be investigated to ascertain the molecular basis for channel pore properties, channel permeation and block, and channel rectification. Aim 2. The structure of the channel polypeptide across the cell membrane will be determined. Aim 3. The subunit composition of the channels will be elucidated, and the domains responsible for channel assembly will be ascertained. The results of these studies will provide new information about the molecular mechanisms involved in the function of the inward rectifier channels in the heart and brain. An understanding of the molecular architecture and function of the K1 channels will enable the development of K1 channel therapeutic agents to treat cardiovascular and neuronal disease.
期刊论文(16)
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DOI: 10.1074/jbc.m106555200
发表时间: 2001-11-02
期刊: JOURNAL OF BIOLOGICAL CHEMISTRY
影响因子: 4.8
作者: [Conti, LR, Radeke, CM, Vandenberg, CA]
通讯作者: Vandenberg, CA
Expression of a putative ATPase suppresses the growth defect of a yeast potassium transport mutant: identification of a mammalian member of the Clp/HSP104 family.
假定的 ATP 酶的表达抑制酵母钾转运突变体的生长缺陷:Clp/HSP104 家族哺乳动物成员的鉴定。
DOI: 10.1016/0378-1119(94)00697-q
发表时间: 1995
期刊: Gene
影响因子: 3.5
作者: [Périer,F, Radeke,CM, Raab-Graham,KF, Vandenberg,CA]
通讯作者: Vandenberg,CA
Assignment of the human hippocampal inward rectifier potassium channel (HIR) gene to 22q13.1.
将人海马内向整流钾通道 (HIR) 基因分配给 22q13.1。
DOI: 10.1016/0888-7543(95)80189-s
发表时间: 1995
期刊: Genomics
影响因子: 4.4
作者: [Budarf,ML, Périer,F, Barnoski,BL, Bell,CJ, Vandenberg,CA]
通讯作者: Vandenberg,CA
DOI: 10.1016/s0006-3495(91)82185-3
发表时间: 1991-12
期刊: Biophysical journal
影响因子: 3.4
作者: [C. Vandenberg;F. Bezanilla]
通讯作者: C. Vandenberg;F. Bezanilla
6
    IDENTIFICATION OF PROTEINS ASSOCIATED WITH INWARD RECTIFIER POTASSIUM CHANNELS
    • 批准号:
      7182427
    • 项目类别:
    • 资助金额:
      $0.4万
    • 财政年份:
      2005
    • 负责人:
      CAROL A VANDENBERG
    • 依托单位:
    INWARD RECTIFIER POTASSIUM CHANNEL ASSOCIATED PROTEINS
    • 批准号:
      6979708
    • 项目类别:
    • 资助金额:
      $0.36万
    • 财政年份:
      2004
    • 负责人:
      CAROL A VANDENBERG
    • 依托单位:
    PDZ Interaction and Inward Rectifier K+ Channel Function
    PDZ Interaction and Inward Rectifier K+ Channel Function
    海外基金