Structural Study of Semaphorins, Neuropilins and Plexins
Structural Study of Semaphorins, Neuropilins and Plexins
批准号:
7569452
负责人:
DIMITAR B NIKOLOV
金额:
$31.91万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-03-06 至 2011-01-31
关键词:
AffinityArchitectureAxonBindingBiochemicalBiological AssayBiological ProcessCell AdhesionCell Surface ReceptorsCellsChemotactic FactorsComplementComplexDataDevelopmentDissociationElementsEquilibriumEventExtracellular ProteinExtracellular StructureFluorescenceFluorescence Resonance Energy TransferGoalsKineticsLengthLifeLigand BindingLigandsMediatingMolecularMultiprotein ComplexesMutationNervous System PhysiologyNeuronsNeuropilinsProcessResearchResolutionRoleSemaphorin-3ASemaphorinsSeriesSignal TransductionSpecificitySpectrum AnalysisStructureSurfaceSystemTherapeutic AgentsTissuesType I Epithelial Receptor CellVascular Endothelial Growth FactorsX-Ray Crystallographyanalytical ultracentrifugationangiogenesisaxon guidancebasedesigninsightmigrationmolecular recognitionplexinreceptorreceptor bindingspinal cord and brain injury
中文摘要
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英文摘要
The semaphorins are a large group of extracellular proteins involved in a variety of processes during
development, including neuronal migration and axon guidance. They function as chemorepellents that
direct axons away from tissues marked by their expression, but in some cases can also act as
chemoattractants. The semaphorin receptors are multiprotein complexes, which include a plexin molecule
serving as the signal-transducing subunit. In addition, some semaphorin receptors include a neuropilin
ligand-binding subunit. Research in this proposal focuses on detailed structural characterization of the
semaphorins, neuropilins, plexins, and their interactions. Preliminary studies of semaphorins and
neuropilins have identified their interacting domains. The crystal structure of the receptor-binding module of
Semaphorin-3A was determined at 2.8 A resolution, revealing an unexpected beta propeller molecular
architecture. X-ray crystallography will be used next to determine the structure of full-length
Semaphorin-3A and structures of selected semaphorins from other classes. The analysis of these
structures will focus on identifying structural elements important for defining the receptor and co-receptor
specificities of semaphorins. The crystal structures of the interacting domains of neuropilins and plexins will
also be determined. Finally, the structures of a series of semaphorin/neuropilin, neuropilin/plexin,
semaphorin/plexin, and semaphorin/neuropilin/plexin complexes will be determined, illuminating the
molecular events leading to the initiation of semaphorin signaling. The structural data will be
complemented by biophysical, biochemical and flourescence/FRET-based studies of the
semaphorin/neuropilin/plexin interactions. The combined structural and biophysical information will provide
fundamental insights into the molecular mechanisms underlying the biological functions of semaphorins,
neuropilins, and plexin, and could have significant applications in development of therapeutic agents for
treatment of brain and spinal cord injuries.
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财政年份:2007
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依托单位:
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海外基金