Molecular Mechanism of Renal Na+ Dependent Cotransport
Molecular Mechanism of Renal Na+ Dependent Cotransport
批准号:
7448555
负责人:
Ana M Pajor
金额:
$31.04万
依托单位国家:
美国
项目类别:
财政年份:
1993
资助国家:
美国
项目状态:
已结题
起止时间:
1993-04-01 至 2011-06-30
关键词:
Acid-Base EquilibriumAffectAffinityAmino AcidsAnionsBindingBiotinylationCarbonCarrier ProteinsCationsCellsCitrateCitratesCitric Acid CycleComplementCoupledCysteineDevelopmentDiseaseEpitheliumEpitopesEscherichia coliFamilyFoundationsFumaratesFutureGrantHealthHelix (Snails)High Blood PressureHomeostasisHomologous GeneHumanIonsKidneyKidney CalculiLabelLaboratoriesLongevityMaintenanceMapsMediatingMembraneMetabolicModelingMolecularMolecular ConformationMutagenesisMutationN-biotinylaminoethyl methanethiosulfonateObesityPathway interactionsPhysiologicalPhysiological ProcessesPlayPropertyProteinsReagentResearchResearch PersonnelRoleScanningSideSite-Directed MutagenesisSourceSpecificityStaphylococcus aureusStructural ModelsStructureSuccinatesTertiary Protein StructureTestingTubular formationVesicleWorkapical membranebaseblood pressure regulationdesigndicarboxylatedicarboxylate-binding proteindirected evolutionear helixinterestmembermutantnovel strategiesprotein structureresearch studysuccinatetool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The low-affinity Na+/dicarboxylate cotransporter NaDC1 is found on the apical membrane of the renal proximal tubular epithelium, where it plays an important role in the reabsorption of citric acid cycle intermediates, including citrate and succinate, from the tubular lumen. The transport activity of NaDC1 affects such important physiological functions as citrate homeostasis (and the development of kidney stones), the regulation of blood pressure, maintenance of acid-base balance, and the overall metabolic status of the body. In our last project period we identified a bacterial homolog of NaDC1, called SdcS, which provides a unique tool in our studies of the SLC13 family. SdcS is a Na+dependent dicarboxylate transporter from Staphylococcus aureus, with 35% identity to NaDC1. The long-term objective of our research is to determine the structural basis of substrate and cation binding and translocation in the Na+/dicarboxylate cotransporters, and to better understand the mechanism of ion-coupled transport. The research plan for our next project period is designed to elucidate the structure and function of NaDC1 and SdcS in four Specific Aims. Aim 1 will use cysteine-scanning mutagenesis to identify the substrate and cation permeation pathway in NaDC1, focusing on transmembrane helices (TM) 7 and 8, predicted to form part of the substrate access channel. Aim 2 will use epitope insertions to test our new 13-TM structural model of NaDCt. Aim 3 will use SdcS as a model transporter to characterize amino acids that are accessible from the inside of the cell during the transport cycle. Finally, Aim 4 will use mutagenic selection to identify the residues required to transport citrate in SdcS. The experiments in this project should provide important information on the members of the SLC13 family and on the ion-coupled mechanism of transport. Our results should lay the foundations to develop future treatments of disorders involving NaDC1. Relevance to human health: NaDC1 is an important transporter for metabolic intermediates (including succinate and citrate) that mediate many physiological processes; thus, NaDC1 may be involved in diseases such as kidney stones, high blood pressure, and obesity. The bacterial homolog, SdcS, is closely related to NaDC1 and allows us to perform experiments that are not possible with the mammalian transporters. Understanding how NaDC1 and SdcS work will help us to develop treatments for NaDC1-mediated diseases.
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Molecular Mechanism of Renal Na+ Dependent Cotransport
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批准号:7921094
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项目类别:
-
资助金额:$16.68万
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财政年份:2009
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负责人:Ana M Pajor
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依托单位:
Involvement of Na/Dicarboxylate Cotransporter in Aging
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批准号:6479293
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项目类别:
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资助金额:$7.45万
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财政年份:2002
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:2697026
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项目类别:
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资助金额:$0.67万
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财政年份:1997
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:2558598
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项目类别:
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资助金额:$0.8万
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财政年份:1997
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负责人:Ana M Pajor
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依托单位:
MECHANISM OF RENAL NA/DICARBOXYLATE TRANSPORT
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批准号:6175973
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项目类别:
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资助金额:$9.34万
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财政年份:1996
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负责人:Ana M Pajor
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依托单位:
MECHANISM OF RENAL NA/DICARBOXYLATE TRANSPORT
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批准号:2904948
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项目类别:
-
资助金额:$9.07万
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财政年份:1996
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负责人:Ana M Pajor
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依托单位:
MECHANISM OF RENAL NA/DICARBOXYLATE TRANSPORT
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批准号:2458696
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项目类别:
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资助金额:$6.46万
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财政年份:1996
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负责人:Ana M Pajor
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依托单位:
MECHANISM OF RENAL NA/DICARBOXYLATE TRANSPORT
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批准号:2134374
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项目类别:
-
资助金额:$6.13万
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财政年份:1996
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负责人:Ana M Pajor
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依托单位:
MECHANISM OF RENAL NA/DICARBOXYLATE TRANSPORT
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批准号:2749400
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项目类别:
-
资助金额:$8.42万
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财政年份:1996
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:2838136
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项目类别:
-
资助金额:$7.8万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:2608452
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项目类别:
-
资助金额:$9.16万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+-DEPENDENT COTRANSPORT
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批准号:2145441
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项目类别:
-
资助金额:$14.79万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
Molecular Mechanism of Renal Na+ Dependent Cotransport
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批准号:6999714
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项目类别:
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资助金额:$34.19万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
Molecular Mechanism of Renal Na+ Dependent Cotransport
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批准号:6835610
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项目类别:
-
资助金额:$35.02万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:6124785
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项目类别:
-
资助金额:$17.69万
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财政年份:1993
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负责人:Ana M Pajor
-
依托单位:
Molecular Mechanism of Renal Na+ Dependent Cotransport
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批准号:6431072
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项目类别:
-
资助金额:$35.02万
-
财政年份:1993
-
负责人:Ana M Pajor
-
依托单位:
Molecular Mechanism of Renal Na+ Dependent Cotransport
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批准号:6621209
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项目类别:
-
资助金额:$35.02万
-
财政年份:1993
-
负责人:Ana M Pajor
-
依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:2016643
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项目类别:
-
资助金额:$16.46万
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财政年份:1993
-
负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+ DEPENDENT COTRANSPORT
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批准号:2850505
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项目类别:
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资助金额:$17.18万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
MOLECULAR MECHANISM OF RENAL NA+-DEPENDENT COTRANSPORT
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批准号:3247718
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项目类别:
-
资助金额:$13.87万
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财政年份:1993
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负责人:Ana M Pajor
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依托单位:
海外基金