2020 Ligand Recognition & Molecular Gating GRC/GRS
2020 Ligand Recognition & Molecular Gating GRC/GRS
批准号:
9913047
负责人:
Alessio Accardi
金额:
$2.0万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-12-01 至 2022-11-30
关键词:
ATP-Binding Cassette TransportersAccountingAddressAgeBindingCardiovascular DiseasesCarrier ProteinsCollaborationsCommunitiesComplexCryoelectron MicroscopyDevelopmentDisabled PersonsDiseaseDrug TargetingEducational process of instructingEndocrine System DiseasesEnsureEquilibriumFemaleFosteringFunctional disorderFutureG-Protein-Coupled ReceptorsGenderGoalsHealthHeart DiseasesHourHumanInterventionIon ChannelIon Channel ProteinItalyJointsLigand BindingLigandsMedicalMembrane ProteinsMetabolic DiseasesMinority ParticipationMolecularMolecular ConformationMyopathyNeuromuscular DiseasesPharmaceutical PreparationsPharmacologic SubstancePhysiologicalPhysiologyPlayPostdoctoral FellowProcessPropertyProtein FamilyProteinsRecruitment ActivityRegulationRenaissanceResearchResearch PersonnelResortRoleScienceScientistSenior ScientistSignal TransductionSlideStructural ProteinStructureTechniquesWomanWorkexperiencegraduate studentimprovedinsightinterestmeetingsmolecular recognitionneglectnervous system disordernovel strategiesparticlepostersprogramsprotein complexprotein functionpublic health relevanceresearch and developmentsolutestructured datasuccesssymposiumtherapeutic targettransmission process
中文摘要
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英文摘要
SUMMARY: The 2020 Gordon Research Conference (GRC) on Ligand Recognition and Molecular
Gating will be held from March 15th-20th at the Renaissance Tuscany Il Ciocco Resort, Italy. The GRC will
be preceded by the related Gordon Research Seminar (GRS), which is organized by and for young
scientists (March 14th-15th). The topic of this GRC/GRS combination is unique, as it addresses the
molecular mechanisms of three important classes of membrane proteins: ion channels, active transporters,
and G-protein coupled receptors (GPCRs). These proteins are central to human physiology and their
dysfunction leads to a large number of neuromuscular, endocrine and metabolic diseases. These proteins
are major therapeutic targets; more than 50% of current drugs on the market target them. Therefore,
elucidating their molecular mechanisms is essential to enable new opportunities for intervention, which
ultimately will lead to improvement of human health. The central focus of this GRC/GRS is on the molecular
mechanisms underlying ligand recognition and binding, ligand-induced conformational changes, solute
transport, regulation of function, and signal transmission. Current focus is on elucidating the structures of
these proteins and on how the structural data illuminates the mechanisms and physiological roles of these
proteins. Our understanding of membrane protein function is undergoing a major leap forward, fueled by
multiple technological breakthroughs, the most important of which is the revolution in electron cryo-
microscopy that led to the determination of several medically important structures of human transporters,
channels and signaling complexes, such as Na+ channels, multidrug ABC transporters and GPCR/G-
protein complexes. Progress has also been made in understanding fundamental processes that are key to
the function of these proteins, such as gating mechanisms of major channels, dynamic rearrangements and
the formation of different signaling complexes. Efforts to identify the function of uncharacterized membrane
protein families are also underway to understand their function in human physiology and disease.
This GRC is unique as it brings together scientists who work on these three different classes of
membrane proteins and are located on different continents, and thus do not meet regularly. They will
benefit tremendously from these interactions as these membrane proteins share common mechanistic
principles and can be studied by a vast array of techniques, many of which will be represented in this
conference. The program will have around 40 speakers, a mix of well-established leaders in the field,
young investigators, postdocs and graduate students. Nine speaker sessions and several poster sessions
will address the major properties of transporters, ion channels, and GPCRs. The GRC/GRS on Ligand
Recognition and Molecular Gating will provide a platform for the presentation and discussion of latest
research results and for the establishment of new collaborations.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Atomic basis for chloride channel and transporter gating and selectivity
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批准号:10319992
-
项目类别:
-
资助金额:$32.35万
-
财政年份:2019
-
负责人:Alessio Accardi
-
依托单位:
Atomic basis for chloride channel and transporter gating and selectivity
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批准号:10083219
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项目类别:
-
资助金额:$32.35万
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财政年份:2019
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负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
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批准号:8860199
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项目类别:
-
资助金额:$51.4万
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财政年份:2014
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负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
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批准号:10170367
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项目类别:
-
资助金额:$41.53万
-
财政年份:2014
-
负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
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批准号:10624809
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项目类别:
-
资助金额:$41.53万
-
财政年份:2014
-
负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
-
批准号:10798983
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项目类别:
-
资助金额:$10.77万
-
财政年份:2014
-
负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
-
批准号:9238783
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项目类别:
-
资助金额:$51.4万
-
财政年份:2014
-
负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
-
批准号:8728513
-
项目类别:
-
资助金额:$57.42万
-
财政年份:2014
-
负责人:Alessio Accardi
-
依托单位:
Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteins
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批准号:10406928
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项目类别:
-
资助金额:$41.53万
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财政年份:2014
-
负责人:Alessio Accardi
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依托单位:
Structure and function of chloride channels and transporters
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批准号:7802969
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项目类别:
-
资助金额:$34.29万
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财政年份:2009
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负责人:Alessio Accardi
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依托单位:
Structure and function of chloride channels and transporters
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批准号:8243567
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项目类别:
-
资助金额:$33.9万
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财政年份:2009
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负责人:Alessio Accardi
-
依托单位:
Structure and function of chloride channels and transporters
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批准号:8450114
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项目类别:
-
资助金额:$32.69万
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财政年份:2009
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负责人:Alessio Accardi
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依托单位:
Structure and function of chloride channels and transporters
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批准号:8101423
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项目类别:
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资助金额:$15.24万
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财政年份:2009
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负责人:Alessio Accardi
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依托单位:
Structure and function of chloride channels and transporters
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批准号:8141955
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项目类别:
-
资助金额:$33.93万
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财政年份:2009
-
负责人:Alessio Accardi
-
依托单位:
海外基金