Mechanisms & Energetics of Transmembrane-induced Signaling of Cytokine Receptors
Mechanisms & Energetics of Transmembrane-induced Signaling of Cytokine Receptors
批准号:
8681468
负责人:
Wonpil Im
金额:
$27.92万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-01 至 2016-06-30
关键词:
AddressAreaBindingBiologicalBiological ModelsBiologyCell membraneCell surfaceCysteineCytokine ReceptorsDataDisulfidesElectron Spin Resonance SpectroscopyEventExtracellular DomainFeedbackFree EnergyGeometryHealthHormonesHumanLigand BindingLigandsLinkMeasuresMembraneMembrane ProteinsMethodsModelingMolecularMolecular ConformationPositioning AttributeProcessProlactin ReceptorReceptor ActivationRoleSequence HomologySideSignal TransductionSimulateSiteSpin LabelsStructureSystemTestingTransmembrane Domainbasecytokinedimerdisulfide bondextracellularfoothuman GHR proteininnovationinterestinterfacialmembrane modelmolecular dynamicsmultidisciplinaryreceptorresearch studyresponserestraintsimulation
中文摘要
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英文摘要
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.
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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
Molecular dynamics studies of ion permeation in VDAC.
VDAC 中离子渗透的分子动力学研究。
DOI:
10.1016/j.bpj.2010.12.3711
发表时间:
2011
期刊:
Biophysical journal
影响因子:
3.4
作者:
[Rui,Huan, Lee,KyuIl, Pastor,RichardW, Im,Wonpil]
通讯作者:
Im,Wonpil
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