课题基金 / 基金详情

REGULATORY MECHANISMS OF PROTEIN TYROSINE PHOSPHATASES

REGULATORY MECHANISMS OF PROTEIN TYROSINE PHOSPHATASES
蛋白质酪氨酸磷酸酶的调控机制
批准号:
2100545
负责人:
HARRY CHARBONNEAU
金额:
$10.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1994
资助国家:
美国
项目状态:
已结题
起止时间:
1994-05-01 至 1999-04-30

项目摘要

项目成果

HARRY CHARBONNEAU的其他基金

相关文献

中文摘要
翻译
蛋白酪氨酸磷酸化的稳态水平是依赖的
英文摘要
The steady state level of protein tyrosine phosphorylation is dependent upon the relative activities of protein tyrosine phosphatases (PTPs) and protein tyrosine kinases. Regulation of PTP activity constitutes an important mechanism for controlling cellular functions which are mediated by protein tyrosine phosphorylation such as growth and development. Despite recent progress in identifying new PTPs, relatively little is known about their substrates, regulation, and cellular functions. The broad objective of these proposed studies is to elucidate the regulatory mechanisms that control the biological activities of PTPs. We will investigate the function and regulation of two nonreceptor enzymes, the T-cell PTP and a distinct baculoviral PTP. The substrate preference and intracellular localization of the T-cell PTP are regulated by its C- terminal domain. Using in vitro mutagenesis, we will determine the location of specific sites within the C-terminal domain that act to regulate substrate specificity. Immunofluorescence will be used to determine the precise intracellular site where the T-cell PTP is localized. Mutagenesis of a hydrophobic, C-terminal segment will be used to determine whether it is responsible for localization of the enzyme. We have identified a PTP (BVP)that is encoded by a baculovirus, Autographa californica. BVP and two cellular homologs comprise a new subfamily of enzymes. We will investigate the function, mechanism of regulation, and substrates of the BVP by analyzing its role in viral function. It is important to determine whether mammalian forms of this subfamily exist and if so, to define their role in controlling tyrosine phosphorylation. We have evidence for the existence of a human homolog and will isolate a cDNA clone encoding it so that it can be expressed and characterized. Aberrant tyrosine phosphorylation resulting from the unregulated activity of oncogenic tyrosine kinases is thought to be an important event leading to cellular transformation. Knowledge of PTP regulation is crucial to understanding how the delicate balance between protein tyrosine kinases and PTPs is maintained during both oncogenesis and normal cell growth. Information gained about the function and regulation of PTPs may lead to the development of methods for manipulating the level of tyrosine phosphorylation that may have application in research and treatment of diseases such as cancer.
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REGULATORY MECHANISMS OF PROTEIN TYROSINE PHOSPHATASES
  • 批准号:
    2100547
  • 项目类别:
  • 资助金额:
    $10.42万
  • 财政年份:
    1994
  • 负责人:
    HARRY CHARBONNEAU
  • 依托单位:
REGULATORY MECHANISMS OF PROTEIN TYROSINE PHOSPHATASES
  • 批准号:
    2414266
  • 项目类别:
  • 资助金额:
    $10.29万
  • 财政年份:
    1994
  • 负责人:
    HARRY CHARBONNEAU
  • 依托单位:
FUNCTION AND REGULATION OF THE CDC14 PROTEIN PHOSPHATASE
  • 批准号:
    6172068
  • 项目类别:
  • 资助金额:
    $22.27万
  • 财政年份:
    1994
  • 负责人:
    HARRY CHARBONNEAU
  • 依托单位:
REGULATORY MECHANISMS OF PROTEIN TYROSINE PHOSPHATASES
  • 批准号:
    2540197
  • 项目类别:
  • 资助金额:
    $3.28万
  • 财政年份:
    1994
  • 负责人:
    HARRY CHARBONNEAU
  • 依托单位: