Functional expression of CFTR and other multidomain proteins
Functional expression of CFTR and other multidomain proteins
批准号:
7739851
负责人:
Neil A Bradbury
金额:
$26.95万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-01 至 2011-07-31
关键词:
AddressAffectCell membraneCell physiologyCellsClassificationCodeCodon NucleotidesCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDiseaseDrug DesignEffectivenessEmbryoFactor AnalysisGenesHereditary DiseaseHumanMembraneMembrane ProteinsMessenger RNAMethodsMolecularMutationPhysiologic pulsePlasmidsProteinsRelative (related person)ResearchResolutionStructureSystemTertiary Protein StructureTestingTimeTranslationsWaterbasedesigninterestkidney cellmutantnovelpatch clampprotein expressionprotein foldingprotein structure functionpublic health relevanceresearch study
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): High-resolution structure determination of proteins is critical in understanding the molecular mechanisms of cellular function. The greatest occurrences within genetic diseases are mutations that alter the structure/function of proteins. A major obstacle for obtaining the high-resolution structure of wild type and mutant proteins is the difficulty in expressing proteins of interest in either a homologous or heterologous system at levels needed for structural studies. The current methods for expressing soluble, and especially membrane, proteins rely on fortuity as much as rational design. The inability to over express proteins can be enigmatic and can be a major block for structure determination. The cystic fibrosis transmembrane conductance regulator (CFTR) is a prime example of a critical protein whose structural analysis has been restricted by the inability to express large amounts of the protein. This project will test a novel hypothesis, which directly addresses the cause for low expression of proteins. CFTR is an ideal protein to use to test this hypothesis most importantly because CFTR is predicted by the hypothesis to be difficult to express at high levels. Thus, expression of CFTR at high levels and controls, which reduced expression of CFTR, would be critical tests for the hypothesis. In addition, CFTR is critical and mutations within it are responsible for a major worldwide disease. Overall, if successful, the results of this project will have a high impact on the biomedical field including research on cystic fibrosis. PUBLIC HEALTH RELEVANCE: Rational drug design based on the high resolution structure of novel and known proteins requires systems for high level expression of the proteins. The high level expression of functional protein is a limiting factor for analysis of most membrane proteins, including the protein defective in cystic fibrosis, CFTR. This project will test a novel hypothesis, which if correct will provide a rational approach for successful expression of multidomain proteins with CFTR being used as the test case.
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会议论文
Role of LMTK2 in CFTR Trafficking
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批准号:8197503
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项目类别:
-
资助金额:$38.5万
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财政年份:2010
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负责人:Neil A Bradbury
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依托单位:
Role of LMTK2 in CFTR Trafficking
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批准号:8039716
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项目类别:
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资助金额:$36.88万
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财政年份:2010
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负责人:Neil A Bradbury
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依托单位:
Role of LMTK2 in CFTR Trafficking
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批准号:8586541
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项目类别:
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资助金额:$37.73万
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财政年份:2010
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负责人:Neil A Bradbury
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依托单位:
Role of LMTK2 in CFTR Trafficking
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批准号:8386586
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项目类别:
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资助金额:$36.65万
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财政年份:2010
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负责人:Neil A Bradbury
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依托单位:
Functional expression of CFTR and other multidomain proteins
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批准号:7904914
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项目类别:
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资助金额:$15.4万
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财政年份:2009
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负责人:Neil A Bradbury
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依托单位:
CFTR REGULATION BY TARGETED KINASE AND PHOSPHATASE
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批准号:6654123
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项目类别:
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资助金额:$12.41万
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财政年份:2002
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负责人:Neil A Bradbury
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依托单位:
Mechanisms of CFTR Internalization
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批准号:6371117
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项目类别:
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资助金额:$23.61万
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财政年份:2001
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负责人:Neil A Bradbury
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依托单位:
Mechanisms of CFTR Internalization
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批准号:6788292
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项目类别:
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资助金额:$23.39万
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财政年份:2001
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负责人:Neil A Bradbury
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依托单位:
Mechanisms of CFTR Internalization
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批准号:6524255
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项目类别:
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资助金额:$23.53万
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财政年份:2001
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负责人:Neil A Bradbury
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依托单位:
CFTR REGULATION BY TARGETED KINASE AND PHOSPHATASE
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批准号:6499598
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项目类别:
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资助金额:$12.41万
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财政年份:2001
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负责人:Neil A Bradbury
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依托单位:
Mechanisms of CFTR Internalization
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批准号:6647747
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项目类别:
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资助金额:$23.45万
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财政年份:2001
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负责人:Neil A Bradbury
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依托单位:
CFTR REGULATION BY TARGETED KINASE AND PHOSPHATASE
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批准号:6358021
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项目类别:
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资助金额:$14.22万
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财政年份:2000
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负责人:Neil A Bradbury
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依托单位:
CFTR REGULATION BY TARGETED KINASE AND PHOSPHATASE
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批准号:6468000
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项目类别:
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资助金额:$12.41万
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财政年份:2000
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负责人:Neil A Bradbury
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依托单位:
MOLEC BIO & GENE EXPRESS CORE, CYSTIC FIBROSIS RES DVMT CENTER, UNIV OF PITTS
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批准号:6319785
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项目类别:
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资助金额:$0.13万
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财政年份:1999
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负责人:Neil A Bradbury
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依托单位:--
CFTR REGULATION BY TARGETED KINASE AND PHOSPHATASE
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批准号:6194476
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项目类别:
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资助金额:$14.22万
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财政年份:1999
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负责人:Neil A Bradbury
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依托单位:
MOLECULAR BIOLOGY & GENE EXPRESSION CORE, U PGH CYSTIC FIBROSIS RES DVMT CTR
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批准号:6282552
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项目类别:
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资助金额:$1.19万
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财政年份:1998
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负责人:Neil A Bradbury
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依托单位:
MOLECULAR BIOLOGY & GENE EXPRESSION CORE, U PGH CYSTIC FIBROSIS RES DVMT CTR
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批准号:6295207
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项目类别:
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资助金额:$1.19万
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财政年份:1998
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负责人:Neil A Bradbury
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依托单位:
MOLECULAR BIOLOGY & GENE EXPRESSION CORE, U PGH CYSTIC FIBROSIS RES DVMT CTR
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批准号:6122517
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项目类别:
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资助金额:$0.0万
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财政年份:1998
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负责人:Neil A Bradbury
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依托单位:
MOLECULAR MECHANISMS OF ENDOCYTIC CFTR RETRIEVAL
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批准号:2147742
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项目类别:
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资助金额:$15.07万
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财政年份:1995
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负责人:Neil A Bradbury
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依托单位:
MOLECULAR MECHANISMS OF ENDOCYTIC CFTR RETRIEVAL
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批准号:2414861
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项目类别:
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资助金额:$15.63万
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财政年份:1995
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负责人:Neil A Bradbury
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依托单位:
海外基金