Diversity Supplement for Spatial Organization of the Mitochondrial Inner Membrane
Diversity Supplement for Spatial Organization of the Mitochondrial Inner Membrane
批准号:
10357501
负责人:
Jonathan R. Friedman
金额:
$1.86万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-09-01 至 2025-08-31
关键词:
AddressAlzheimer&aposs DiseaseArchitectureCell RespirationCell physiologyCellsComplexCrista ampullarisDefectDevelopmentDiseaseElementsFutureGenerationsGoalsHomeostasisHumanInner mitochondrial membraneIonsLeadLinkMembraneMitochondriaMolecularMorphogenesisMorphologyNeurodegenerative DisordersNucleotidesOrganellesOxidative PhosphorylationParkinson DiseasePhenotypePhospholipidsPositioning AttributeProductionResearchRespirationRoleSiteStructureSystemTherapeuticWorkYeastsamino acid metabolismgenetic approachhuman diseaseinsightmitochondrial dysfunctionmitochondrial membranenovelprograms
中文摘要
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英文摘要
Project Summary
Mitochondria are double-membrane bound organelles that perform many crucial cellular functions, including
nucleotide and amino acid metabolism, cellular phospholipid and ion homeostasis, and their most notorious
function, generation of cellular energy via oxidative phosphorylation. Mitochondrial form and function are tightly
linked. The ability of the organelle to efficiently perform respiration depends on the correct spatial organization
of the mitochondrial inner membrane into elaborately shaped morphological domains, including cristae, the
hallmark of the organelle. Cristae morphology defects lead to reduced cellular respiration and is a phenotypic
consequence of a number of diseases, including neurodegenerative disorders such as Alzheimer’s and
Parkinson’s Disease. Despite their importance, we have minimal mechanistic understanding of how cristae are
formed and organized within the organelle. Recently, the Mitochondrial Contact Site and Cristae Organizing
System (MICOS) complex was identified as a master regulator of spatial organization of mitochondria. I
previously determined that MICOS is organized into two non-redundant subcomplexes that independently
assemble and localize to cristae junctions, a key structural element of the mitochondrial inner membrane.
Despite our progress, we have minimal mechanistic understanding of how MICOS contributes to the number,
position, and morphogenesis of cristae membranes. We will address these deficits by exploring the molecular
basis of MICOS function in yeast cells and, using candidate and forward genetic strategies, determine how
MICOS is regulated to fine tune cristae architecture in human cells. This work will lead to insight into the spatial
organization of mitochondria and the form-function relationship of the organelle, provide the basis for the future
development of my research program, and give us molecular insight into the disorganization of mitochondrial
membranes that occurs as a consequence of a number of human diseases.
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Spatial Organization of the Mitochondrial Inner Membrane
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批准号:10229557
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项目类别:
-
资助金额:$41.0万
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财政年份:2020
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负责人:Jonathan R. Friedman
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依托单位:
Spatial Organization of the Mitochondrial Inner Membrane
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批准号:10469391
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项目类别:
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资助金额:$41.0万
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财政年份:2020
-
负责人:Jonathan R. Friedman
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依托单位:
Spatial Organization of the Mitochondrial Inner Membrane
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批准号:10674219
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项目类别:
-
资助金额:$5.58万
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财政年份:2020
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负责人:Jonathan R. Friedman
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依托单位:
Spatial Organization of the Mitochondrial Inner Membrane
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批准号:10683127
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项目类别:
-
资助金额:$41.0万
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财政年份:2020
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负责人:Jonathan R. Friedman
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依托单位:
Spatial Organization of the Mitochondrial Inner Membrane
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批准号:10026824
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项目类别:
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资助金额:$40.88万
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财政年份:2020
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负责人:Jonathan R. Friedman
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依托单位:
Spatial Organization of the Mitochondrial Inner Membrane
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批准号:10467263
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项目类别:
-
资助金额:$7.45万
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财政年份:2020
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负责人:Jonathan R. Friedman
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依托单位:
Regulation of Mitochondrial Inner Membrane Organization
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批准号:9334933
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项目类别:
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资助金额:$15.42万
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财政年份:2016
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负责人:Jonathan R. Friedman
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依托单位:
Regulation of mitochondrial inner membrane organization
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批准号:9606265
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项目类别:
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资助金额:$24.9万
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财政年份:2016
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负责人:Jonathan R. Friedman
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依托单位:
Regulation of Mitochondrial Inner Membrane Organization
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批准号:9162338
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项目类别:
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资助金额:$15.37万
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财政年份:2016
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负责人:Jonathan R. Friedman
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依托单位: