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SERPIN GENETICS STRUCTURE AND FUNCTION

SERPIN GENETICS STRUCTURE AND FUNCTION
Serpin 遗传学结构和功能
批准号:
3341763
负责人:
SUSAN C BOCK
金额:
$17.37万
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-10-01 至 1995-06-30

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中文摘要
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英文摘要
The long term goal of this project is to understand serpin (serine protease inhibitor) structure/function relationships by studying naturally occurring and in vitro generated serpin mutants. Improved understanding of serpin structure/function principles will lead to more effective treatment for thrombosis, bleeding, permeability and pulmonary disorders associated with serpin/protease imbalances. Specific Aim 1 is to determine why perturbations of the P12 region change a serpin from an inhibitor to a substrate. The P12 region is located on the amino terminal side of the reactive center. Analysis of naturally occurring serpin mutants indicates that the P12 region is involved in determining whether a serpin is an inhibitor or a substrate for its target protease(s). A model for the role of the P12 region in determining serpin inhibitor/substrate status is proposed and will be tested by studying the interactions of normal serpins and P12 region mutants with proteases. Specific Aim 2 is to determine why integrity of the ATIII P11' region is required to obtain normal circulating levels of a serpin. The P11' region is located on the carboxy terminal side of the reactive center. Naturally occurring serpin mutants with lesions in the P11' region are present at extremely reduced levels in the circulation, suggesting that it is important for determining intracellular degradation, secretion or clearance rates. These parameters will be studied in cells expressing normal serpins and Pll' region mutants in order to elucidate the role the Pll' region plays in determining circulating serpin levels. Specific Aim 3 is to elucidate the structural basis of antithrombin III heparin cofactor activity. A model for ATIII heparin cofactor activity is proposed and will be tested by making antithrombin mutants with defined structural abnormalities and studying their functional properties. A further test of the model will involve trying to transfer the heparin cofactor property of antithrombin III to another serpin, such as alpha 1-antitrypsin.
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Development of Cross Protective H5 Hemagglutinin Antigens
  • 批准号:
    8072917
  • 项目类别:
  • 资助金额:
    $1.14万
  • 财政年份:
    2010
  • 负责人:
    SUSAN C BOCK
  • 依托单位:
Development of Cross Protective H5 Hemagglutinin Antigens
  • 批准号:
    7880704
  • 项目类别:
  • 资助金额:
    $18.62万
  • 财政年份:
    2009
  • 负责人:
    SUSAN C BOCK
  • 依托单位:
Development of Cross Protective H5 Hemagglutinin Antigens
  • 批准号:
    7741349
  • 项目类别:
  • 资助金额:
    $22.58万
  • 财政年份:
    2009
  • 负责人:
    SUSAN C BOCK
  • 依托单位:
Conformational change propagation in ATIII-heparin
  • 批准号:
    7331505
  • 项目类别:
  • 资助金额:
    $31.89万
  • 财政年份:
    2005
  • 负责人:
    SUSAN C BOCK
  • 依托单位:
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