Structure and regulation of non-receptor tyrosine kinases
Structure and regulation of non-receptor tyrosine kinases
批准号:
9247783
负责人:
MICHAEL J ECK
金额:
$41.52万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-08-10 至 2019-03-31
关键词:
Active SitesArchitectureAsthmaAutoimmune ProcessBindingBinding SitesBiochemistryBiosensorCell Differentiation processCell LineCell ProliferationCellsCellular biologyChemistryComplexCrystallizationCysteineCytokine ReceptorsCytoplasmic TailDiseaseDrug TargetingElectron MicroscopyElementsErythrocytesErythropoietinErythropoietin ReceptorFamilyFamily memberFluorescence Resonance Energy TransferFocal Adhesion Kinase 1GoalsGray unit of radiation doseGrowth Factor ReceptorsHealthHematopoietic NeoplasmsHumanIn VitroIndividualInduced MutationInflammatoryIntegrinsInterferonsInterleukinsInvadedJanus kinaseLengthLeukocytesMalignant NeoplasmsMolecular ConformationMutagenesisMutationMyeloproliferative diseaseNeoplasm MetastasisNormal tissue morphologyPhospholipidsPhosphotransferasesPlayProductionPropertyProtein Tyrosine KinaseProteinsRegulationReportingRheumatoid ArthritisRoleSH3 DomainsSignal TransductionSiteSomatotropinSpecificityStimulusStructureSurfaceT-LymphocyteTEC Protein Tyrosine KinaseTestingTyrosine Kinase DomainWorkX-Ray Crystallographybasecell motilitycytokinedesigndrug developmentimprovedinhibitor/antagonistinsightmigrationmutantnovelnovel therapeuticsreceptorresponsesrc Homology Region 2 Domainstructural biologytool
中文摘要
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英文摘要
Non-receptor tyrosine kinases (NRTKs) function as tightly regulated, integrating switches in cellular signal
transduction. Here we focus on representatives of three NRTK families, which have distinct multi-domain
architectures: Jak-family kinases, Focal Adhesion Kinase (FAK), and the Tec-family member ITK (Il-2 inducible
tyrosine kinase). Our longterm goals are to elucidate autoregulatory mechanisms of NRTKs at a structural
level, to understand how these regulatory mechanisms are disrupted in cancer, and to use structural insights to
facilitate discovery of novel inhibitors. With our collaborators, we are combining the tools of structural biology,
biochemistry, cell biology, and chemistry in a unified way to advance these goals. We propose three Specific
Aims. First, we will discover how Jak kinases recognize their cognate cytokine receptors and how they are
regulated by interactions among their constituent domains. We have crystallized an Nterminal fragment of
Jak2, and have also prepared a complex of this portion of Jak2 with the cytoplasmic tail of the erythropoietin
receptor for structural analysis. Our studies of Jak regulation build on our recently determined structure of a
linker/pseudokinase regulatory module, and through elucidation of the structure of essentially full-length Jak2,
we will explain how the this module controls the activity of the adjacent kinase domain, and how this control is
disrupted by the V617F mutation in myeloproliferative neoplasms. Second, we will determine structurally how
focal adhesion kinase (FAK) is activated by PI(4,5)P2. This aim builds on our determination of the structure of
FAK in its autoinhibited state, and our discovery that it binds and is activated by the PI(4,5)P2. Third, we will
elucidate the structure an SH3-SH2-kinase fragment of Itk in order to understand its regulation and to facilitate
inhibitor discovery. Based on our structural insights, we are developing irreversible inhibitors specific for Jak3
that may be useful in treatment of autoimmune and inflammatory disorders.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
Crystal Structure of the FERM-SH2 Module of Human Jak2.
人类JAK2的FERM-SH2模块的晶体结构。
DOI:
10.1371/journal.pone.0156218
发表时间:
2016
期刊:
PloS one
影响因子:
3.7
作者:
[McNally R, Toms AV, Eck MJ]
通讯作者:
Eck MJ
DOI:
10.1021/acs.jmedchem.5b00710
发表时间:
2015-08-27
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Tan L, Akahane K, McNally R, Reyskens KM, Ficarro SB, Liu S, Herter-Sprie GS, Koyama S, Pattison MJ, Labella K, Johannessen L, Akbay EA, Wong KK, Frank DA, Marto JA, Look TA, Arthur JS, Eck MJ, Gray NS]
通讯作者:
Gray NS
Small molecule inhibitors with a therapeutic window for EGFR signaling variants in glioblastoma
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批准号:10306230
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项目类别:
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资助金额:$19.62万
-
财政年份:2021
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负责人:MICHAEL J ECK
-
依托单位:
Small molecule inhibitors with a therapeutic window for EGFR signaling variants in glioblastoma
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批准号:10491835
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项目类别:
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资助金额:$17.78万
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财政年份:2021
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负责人:MICHAEL J ECK
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依托单位:
Structure, mechanism, and pharmacology of BRAF and its partners in the RAS/RAF/MAP kinase pathway
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批准号:9816771
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项目类别:
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资助金额:$106.8万
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财政年份:2019
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负责人:MICHAEL J ECK
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依托单位:
Structure, mechanism, and pharmacology of BRAF and its partners in the RAS/RAF/MAP kinase pathway
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批准号:10669154
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项目类别:
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资助金额:$104.66万
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财政年份:2019
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负责人:MICHAEL J ECK
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依托单位:
Structure, mechanism, and pharmacology of BRAF and its partners in the RAS/RAF/MAP kinase pathway
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批准号:10212985
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项目类别:
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资助金额:$106.8万
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财政年份:2019
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负责人:MICHAEL J ECK
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依托单位:
Structure, mechanism, and pharmacology of BRAF and its partners in the RAS/RAF/MAP kinase pathway
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批准号:10471180
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项目类别:
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资助金额:$104.66万
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财政年份:2019
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负责人:MICHAEL J ECK
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依托单位:
Discovery and optimization of novel mutant-selective allosteric inhibitors of EGFR T790M
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批准号:10534760
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项目类别:
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资助金额:$48.07万
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财政年份:2015
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负责人:MICHAEL J ECK
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依托单位:
Discovery and optimization of novel mutant-selective allosteric inhibitors of EGFR T790M
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批准号:10316246
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项目类别:
-
资助金额:$48.07万
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财政年份:2015
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负责人:MICHAEL J ECK
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依托单位:
Discovery and optimization of novel mutant-selective allosteric inhibitors of EGFR T790M
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批准号:9188065
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项目类别:
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资助金额:$42.59万
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财政年份:2015
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负责人:MICHAEL J ECK
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依托单位:
Structure and regulation of non-receptor tyrosine kinases
-
批准号:9037683
-
项目类别:
-
资助金额:$41.52万
-
财政年份:2014
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负责人:MICHAEL J ECK
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依托单位:
Structure and regulation of non-receptor tyrosine kinases
-
批准号:8671897
-
项目类别:
-
资助金额:$41.52万
-
财政年份:2014
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负责人:MICHAEL J ECK
-
依托单位:
Project 1--Targeted therapies for pediatric low-grade astrocytoma (Eck/Wright/Haas)
-
批准号:10696099
-
项目类别:
-
资助金额:$31.76万
-
财政年份:2013
-
负责人:MICHAEL J ECK
-
依托单位:
Structure
-
批准号:8237132
-
项目类别:
-
资助金额:$29.89万
-
财政年份:2012
-
负责人:MICHAEL J ECK
-
依托单位:
Core B: Structure and Biochemistry
-
批准号:10231103
-
项目类别:
-
资助金额:$24.05万
-
财政年份:2012
-
负责人:MICHAEL J ECK
-
依托单位:
MOLECULAR INTERACTIONS REGULATING INTRACELLULAR SIGNALING
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批准号:8361664
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项目类别:
-
资助金额:$1.83万
-
财政年份:2011
-
负责人:MICHAEL J ECK
-
依托单位:
STRUCTURAL STUDIES OF THE ACTIN ORGANIZERS SPIRE AND FMN2
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批准号:8169209
-
项目类别:
-
资助金额:$1.8万
-
财政年份:2010
-
负责人:MICHAEL J ECK
-
依托单位:
CRYSTAL STRUCTURE OF DRUG-RESISTANT EGFR MUTANT IN COMPLEX WITH NEW INHIBITORS
-
批准号:8169315
-
项目类别:
-
资助金额:$4.32万
-
财政年份:2010
-
负责人:MICHAEL J ECK
-
依托单位:
CRYSTAL STRUCTURE OF A COILED COIL DOMAIN OF HUMAN P160ROCK
-
批准号:8169314
-
项目类别:
-
资助金额:$4.69万
-
财政年份:2010
-
负责人:MICHAEL J ECK
-
依托单位:
MACCHESS PROGRAM FOR MICROCRYSTALLOGRAPHY/MEMBRANE PROTEIN CRYSTALS
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批准号:7955588
-
项目类别:
-
资助金额:$0.67万
-
财政年份:2009
-
负责人:MICHAEL J ECK
-
依托单位:
STRUCTURAL BIOLOGY OF SIGNALING AND THE ACTIN CYTOSKELETON
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批准号:7955079
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项目类别:
-
资助金额:$7.93万
-
财政年份:2009
-
负责人:MICHAEL J ECK
-
依托单位:
海外基金