MECHANISM OF ION TRANSPORT THROUGH MEMBRANE CHANNELS

离子通过膜通道的传输机制

基本信息

  • 批准号:
    3286971
  • 负责人:
  • 金额:
    $ 6.47万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1984
  • 资助国家:
    美国
  • 起止时间:
    1984-09-01 至 1987-08-31
  • 项目状态:
    已结题

项目摘要

The goal of the proposed research is to understand the chemical basis for sodium and potassium fluxes across biological membranes. The questions will be approached using three types of channel-forming molecules of bacterial origin: cidins A, B, and C which associate as dimers to form transmembrane channels; (2) various chemically modified analogues includng covalently coupled homo-and heterodimers, of these same gramicidins which also form active channels, but of different lifetimes and/or ion transport rates from the native molecules; and (3) a larger protein, one of the type El colicins which have recently been shown to form voltage-dependent sodium/potassium channels in the E. coli membrane and in artificial lipid bilayers. The purpose in studying these type of molecules is to establish principles governing possible modes of action of all such channel-forming proteins in biological systems. The results will indicate the molecular basis for the action of ion pumps and gates in membranes, which in turn directly affect (a) a cell's ability to control its ionic composition, transmembrane potential and osmotic pressure, and (b) the conduction of nerve impulses in higher animals. Our previous work has characterized a conformational change which accompanies cation binding to gramicidins A, B, and C. A combination of neutron diffraction and x-ray diffraction are being used to further examine these structures, including the use of isomorphous deuterium-hydrogen substitution to phase reflections in single-crystal neutron diffraction. In addition, the conducting properties of a variety of semisynthetic gramicidin A analogues, in which amino acids having side chains of varying size and polarity have been substituted at the N-terminal, are being examined.
这项拟议研究的目的是了解钠的化学基础

项目成果

期刊论文数量(0)
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Roger E Koeppe其他文献

Roger E Koeppe的其他文献

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{{ truncateString('Roger E Koeppe', 18)}}的其他基金

RESEARCH PILOT PROJECT PROGRAM
研究试点项目计划
  • 批准号:
    8364934
  • 财政年份:
    2011
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIP FOR BIOMED RES IN ARKANSAS: OUTREACH CORE
阿肯色州 BIOMED RES 合作伙伴关系:外展核心
  • 批准号:
    8359801
  • 财政年份:
    2011
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIP FOR BIOMED RES IN ARKANSAS: OUTREACH CORE
阿肯色州 BIOMED RES 合作伙伴关系:外展核心
  • 批准号:
    8168083
  • 财政年份:
    2010
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIPS FOR BIOMEDICAL RESEARCH IN ARKANSAS: SCIENCE RESEARCH CORE
阿肯色州生物医学研究伙伴关系:科学研究核心
  • 批准号:
    8168095
  • 财政年份:
    2010
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIP FOR BIOMED RES IN ARKANSAS: OUTREACH CORE
阿肯色州 BIOMED RES 合作伙伴关系:外展核心
  • 批准号:
    7959420
  • 财政年份:
    2009
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIPS FOR BIOMEDICAL RESEARCH IN ARKANSAS: SCIENCE RESEARCH CORE
阿肯色州生物医学研究伙伴关系:科学研究核心
  • 批准号:
    7959432
  • 财政年份:
    2009
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIPS FOR BIOMEDICAL RESEARCH IN ARKANSAS: SCIENCE RESEARCH CORE
阿肯色州生物医学研究伙伴关系:科学研究核心
  • 批准号:
    7725065
  • 财政年份:
    2008
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIPS FOR BIOMEDICAL RESEARCH IN ARKANSAS: SCIENCE RESEARCH CORE
阿肯色州生物医学研究伙伴关系:科学研究核心
  • 批准号:
    7610011
  • 财政年份:
    2007
  • 资助金额:
    $ 6.47万
  • 项目类别:
PARTNERSHIPS FOR BIOMEDICAL RESEARCH IN ARKANSAS: SCIENCE RESEARCH CORE
阿肯色州生物医学研究伙伴关系:科学研究核心
  • 批准号:
    7381393
  • 财政年份:
    2006
  • 资助金额:
    $ 6.47万
  • 项目类别:
PEPTIDE SYNTHESIS - AMINO ACID ANALYSIS FACILITY
肽合成 - 氨基酸分析设备
  • 批准号:
    3103594
  • 财政年份:
    1992
  • 资助金额:
    $ 6.47万
  • 项目类别:

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MRI:购买 X 射线衍射仪用于化学结构-功能研究的研究和培训
  • 批准号:
    1726630
  • 财政年份:
    2017
  • 资助金额:
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  • 项目类别:
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