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OPTICAL STUDIES OF PROTEIN STRUCTURE/FUNCTION

OPTICAL STUDIES OF PROTEIN STRUCTURE/FUNCTION
蛋白质结构/功能的光学研究
批准号:
2021773
负责人:
LUBERT STRYER
金额:
$23.94万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1979
资助国家:
美国
项目状态:
已结题
起止时间:
1979-01-01 至 2001-03-31

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中文摘要
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英文摘要
The structure and mechanism of action of a family of myristoylated calcium-sensing proteins, exemplified by retinal recoverin, will be investigated by fluorescence, NMR, and spin-label spectroscopy. These acylated proteins move from the cytosol to a membrane on binding calcium. The aim is to determine the molecular mechanism of calcium-myristoyl switches and define their roles in signal transduction processes. Having solved the three-dimensional structures of calcium-free myristoylated recoverin and calcium-bound unmyristoylated recoverin, we turn now to the determination of the structure of the calcium-bound form of myristoylated recoverin to reveal the precise structural basis of the switch. Our working hypothesis is that recoverin and brain homologs such as neurocalcin and hippocalcin serve to couple calcium cascades to G-protein cascades by interacting with kinases that deactivate seven-helix receptors. The membrane-contact sites of recoverin in the Ca2+-bound state and their depth will be determined by spin-label ESR spectroscopy using nitroxide-labeled myristate and nitroxide-tagged cysteines introduced by mutagenesis. Structural, spectroscopic, and functional studies of the interaction of Ca2+-bound recoverin with rhodopsin kinase and fragments of this target will also be carried out. Three classes of recoverin mutants will be generated and analyzed to further our understanding of the structure and dynamics of this sensor: (1) Nonpolar residues in the myristoyl binding pocket will be replaced by polar ones. (2) Glycines in putative hinge regions will be changed to alanine. (3) Charged residues surrounding a concave hydrophobic surface, the putative target-binding site, will be charged to oppositely-charged residues. Structural studies of neurocalcin and hippocalcin will also be carried out and targets of these brain homologs will be identified using the yeast two-hybrid system. A yeast homolog will be expressed and analyzed to provide insight into the evolution of this family of neuronal calcium sensors.
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MECHANISM OF CALCIUM SPIKING IN SIGNAL TRANSDUCTION
  • 批准号:
    3384994
  • 项目类别:
  • 资助金额:
    $19.99万
  • 财政年份:
    1989
  • 负责人:
    LUBERT STRYER
  • 依托单位:
MECHANISM OF CALCIUM SPIKING IN SIGNAL TRANSDUCTION
  • 批准号:
    3384998
  • 项目类别:
  • 资助金额:
    $21.07万
  • 财政年份:
    1989
  • 负责人:
    LUBERT STRYER
  • 依托单位:
MECHANISM OF CALCIUM SPIKING IN SIGNAL TRANSDUCTION
  • 批准号:
    3384995
  • 项目类别:
  • 资助金额:
    $17.56万
  • 财政年份:
    1989
  • 负责人:
    LUBERT STRYER
  • 依托单位:
MECHANISM OF CALCIUM SPIKING IN SIGNAL TRANSDUCTION
  • 批准号:
    3384996
  • 项目类别:
  • 资助金额:
    $18.92万
  • 财政年份:
    1989
  • 负责人:
    LUBERT STRYER
  • 依托单位:
国内基金
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  • 项目类别:
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  • 资助金额:
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  • 批准年份:
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  • 负责人:
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  • 依托单位:
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  • 批准号:
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  • 批准年份:
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  • 依托单位: