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DESCRIPTION (provided by applicant): How transmembrane (TM) domains of membrane proteins transmit the signal across the cell membrane has long been a subject of keen interest in biology. There is a recent paradigm shift in the mechanism of activation for the cytokine receptor superfamily. The role of cytokine hormone binding to the extracellular domain is now recognized as an "inducer" of the conformational change of pre-dimerized TM domains that triggers subsequent intracellular responses. This is drastically different from its traditional role as an "organizer" whose sole function was to initiate the receptor TM dimer formation. Our long-term objective is to delineate the mechanisms and accompanying energetics of TM-induced signaling of various single-pass TM receptors during the inactive to active transition upon ligand binding. Our hypothesis is that the inactive off-state conformation is much more stable than the active on-state one, and the major role of ligand binding is to disrupt the pre-dimerized (energetically stable) TM-TM contact that locks-in the off-state structure, to direct the (energetically unstable) on-state structure. In this proposal, we will use human growth hormone receptor (hGHR) and human prolactin receptor (hPRLR) as prototypical model systems for homodimeric TM-induced activation. The objectives of this proposal are to determine the interfacial residues of hGHR and hPRLR TM dimers and to elucidate the conformational and energetic changes during the activation process by innovative, multidisciplinary combination of versatile computational and experimental approaches. The successful completion of this project will have a significant impact on the field, not only by elucidating the TM signaling mechanism and energetics, but also by providing the computational and experimental methods that can be used to characterize the biological activation process of other cytokine receptors and the plentitude of other single-pass TM receptors, which all have the critical importance to biology and thus, human health.
期刊论文(15)
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会议论文
DOI: 10.1016/j.bpj.2018.01.004
发表时间: 2018-03
期刊: Biophysical journal
影响因子: 3.4
作者: [Soohyung Park;L. Krshnan;M. J. Call;M. Call;W. Im]
通讯作者: Soohyung Park;L. Krshnan;M. J. Call;M. Call;W. Im
DOI: 10.1021/ci300178e
发表时间: 2012-10-22
期刊: Journal of chemical information and modeling
影响因子: 5.6
作者: [Lee HS, Im W]
通讯作者: Im W
DOI: 10.1016/j.bpj.2011.05.030
发表时间: 2011-06
期刊: Biophysical journal
影响因子: 3.4
作者: [Hahnbeom Park;W. Im;Chaok Seok]
通讯作者: Hahnbeom Park;W. Im;Chaok Seok
DOI: 10.1021/ct500504g
发表时间: 2014-07-08
期刊: JOURNAL OF CHEMICAL THEORY AND COMPUTATION
影响因子: 5.5
作者: [Park, Soohyung, Im, Wonpil]
通讯作者: Im, Wonpil
9
    Biophysical characterization of SARS-CoV-2 spike protein - receptor interactions
    • 批准号:
      10286279
    • 项目类别:
    • 资助金额:
      $19.97万
    • 财政年份:
      2021
    • 负责人:
      Wonpil Im
    • 依托单位:
    Biophysical characterization of SARS-CoV-2 spike protein - receptor interactions
    • 批准号:
      10445350
    • 项目类别:
    • 资助金额:
      $22.63万
    • 财政年份:
      2021
    • 负责人:
      Wonpil Im
    • 依托单位:
    CHARMM-GUI Development for Biomolecular Modeling and Simulation Community
    • 批准号:
      10793784
    • 项目类别:
    • 资助金额:
      $13.71万
    • 财政年份:
      2020
    • 负责人:
      Wonpil Im
    • 依托单位:
    CHARMM-GUI Development for Biomolecular Modeling and Simulation Community
    • 批准号:
      10447810
    • 项目类别:
    • 资助金额:
      $32.93万
    • 财政年份:
      2020
    • 负责人:
      Wonpil Im
    • 依托单位:
    国内基金
    海外基金
    层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
    • 批准号:
      2021JJ40433
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2021
    • 负责人:
      孙磊
    • 依托单位:
    寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
    • 批准号:
      32001603
    • 项目类别:
      青年科学基金项目
    • 资助金额:
      24.0万元
    • 批准年份:
      2020
    • 负责人:
      段真珍
    • 依托单位:
    AREA国际经济模型的移植.改进和应用
    • 批准号:
      18870435
    • 项目类别:
      面上项目
    • 资助金额:
      2.0万元
    • 批准年份:
      1988
    • 负责人:
      史树中
    • 依托单位: