Molecular Basis for Aquaporin Conductance
Molecular Basis for Aquaporin Conductance
批准号:
7477234
负责人:
FRANKLIN Alan HAYS
金额:
$5.04万
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:
2006-08-01 至 2009-07-31
关键词:
Active Biological TransportAddressAlcoholsAmmoniaBiologicalBiological AssayBlindnessBrain EdemaCell membraneCellular MembraneClassCommunitiesCoupledCrystallizationCysteineDefectDiffusionDiseaseDisruptionErythrocytesEscherichia coliExhibitsExtravasationFunctional disorderGoalsHumanIn VitroIntegral Membrane ProteinIonsKidneyKnowledgeLibrariesLifeLinkMembraneMembrane PotentialsMolecularMorbidity - disease rateMutagenesisMutationNumbersPlasmodiumPlasmodium falciparumProcessProteinsProtonsRangeRateScreening procedureStructureSulfhydryl CompoundsTherapeuticTissuesWaterbasedesigndrug discoveryinhibitor/antagonistmortalitymutantnervous system disordernovelpreventproteoliposomeswater channel
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Aquaporins (AQPs), a major class of integral membrane proteins found throughout all domains of life, selectively transport water and/or aliphatic alcohols and ammonia across membranes. There are 13 AQPs in humans that exhibit tissue specific expression. Defects in aquaporin function have been linked to a disparate number of human ailments including kidney dysfunction, brain oedema and vision loss. Brain oedema itself is a significant contributor to mortality and morbidity associated with many common neurological disorders. Indeed, disruption of the electrochemical gradient across the cell membranes, generated through active transport, is very disruptive to cellular viability. Thus, understanding the molecular basis for how AQPs function is a key objective within the aquaporin community. The goal of the proposed studies is to understand how AQPs are able to transport water across cellular membranes at near diffusion rates while preserving this electrochemical membrane potential. Mutational studies of AQPZ, one of two aquaporins from Escherichia coli, will be used to address this question. I also propose to facilitate the discovery of inhibitors that are selective for a particular AQP that is key to the red blood cell form of Plasmodium falciparum. Targeting AQPs with therapeutics may become a valuable avenue for combating disease.
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批准号:9753262
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项目类别:
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资助金额:$28.25万
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财政年份:2016
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负责人:FRANKLIN Alan HAYS
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依托单位:
Deciphering ShcA-mediated ROS Production as a Novel Intervention Strategy in Diabetes Therapy
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批准号:9349551
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项目类别:
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资助金额:$28.25万
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财政年份:2016
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Deciphering ShcA-mediated ROS Production as a Novel Intervention Strategy in Diabetes Therapy
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批准号:9193886
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项目类别:
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资助金额:$28.25万
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财政年份:2016
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负责人:FRANKLIN Alan HAYS
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依托单位:
Molecular Basis for Aquaporin Conductance
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批准号:7153307
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项目类别:
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资助金额:$4.6万
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财政年份:2006
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负责人:FRANKLIN Alan HAYS
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依托单位:
Molecular Basis for Aquaporin Conductance
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批准号:7261404
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项目类别:
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资助金额:$4.88万
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财政年份:2006
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负责人:FRANKLIN Alan HAYS
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依托单位:
MOLECULAR DETERMINANTS OF GEMCITABINE (Franklin Hays)
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批准号:9099947
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项目类别:
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资助金额:$20.64万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
Project 4
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批准号:8521832
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项目类别:
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资助金额:$22.2万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
Project 4
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批准号:8542667
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项目类别:
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资助金额:$20.83万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
MOLECULAR DETERMINANTS OF GEMCITABINE (Franklin Hays)
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批准号:8539821
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项目类别:
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资助金额:$20.7万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
Project 4
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批准号:8692938
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项目类别:
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资助金额:$21.08万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
MOLECULAR DETERMINANTS OF GEMCITABINE (Franklin Hays)
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批准号:8461445
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项目类别:
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资助金额:$22.19万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
MOLECULAR DETERMINANTS OF GEMCITABINE (Franklin Hays)
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批准号:8723255
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项目类别:
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资助金额:$21.2万
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财政年份:--
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负责人:FRANKLIN Alan HAYS
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依托单位:
海外基金