Undergrad supplement: Ubiquitin-Dependent Protein Regulation and Quality Control of the Lysosomal Membrane
Undergrad supplement: Ubiquitin-Dependent Protein Regulation and Quality Control of the Lysosomal Membrane
批准号:
10589309
负责人:
Ming Li
金额:
$0.98万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-13 至 2024-08-31
关键词:
AgingAlzheimer&aposs DiseaseAutophagocytosisBiological ModelsCellsComplexDegradation PathwayDevelopmentDigestionDown-RegulationEndocytosisFunctional disorderGoalsHumanHuntington DiseaseInvestigationLaboratoriesLightLysosomal Storage DiseasesLysosomesMammalian CellMembraneMembrane ProteinsMolecularNeurodegenerative DisordersOrganellesParkinson DiseasePathway interactionsPlayProteinsProteomeProteomicsQuality ControlRecyclingRegulationResearchRoleSignal TransductionStressStructureUbiquitinVacuoleYeastscell growthdetection of nutrientexhaustionfollow-uplysosome membranerecruittreatment strategyubiquitin-protein ligaseundergraduate student
中文摘要
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英文摘要
Project Summary
The lysosome is an essential organelle responsible for the digestion and recycling of materials
delivered by endocytosis and autophagy. It also plays important role in nutrient sensing and
control of cell growth by regulating the localization and activity of mTORC1 signaling complex.
Because of its importance, lysosome dysfunction leads to ~ 50 types of lysosomal storage
diseases (LSDs) and contributes to many aging-related neurodegenerative diseases such as
Alzheimer’s, Huntington’s, and Parkinson’s diseases. Despite exhaustive research on how
proteins are delivered to lysosomes, how lysosomes regulate their own membrane proteins
remains poorly understood. However, studying this question will reveal how cells maintain a
healthy lysosome
during stresses and aging.
Our long-term goal is to understand these fundamental questions using both yeast and
mammalian cells as model systems. Recently, we discovered a ubiquitin- and ESCRTdependent
down-regulation pathway for lysosome (vacuole) membrane proteins in yeast.
Follow-up investigations in our laboratory led us to hypothesize that the ubiquitin- and ESCRTdependent
degradation pathway is a general conserved mechanism to regulate the
lysosome membrane composition from yeast to human. Consistently, recent proteomic
studies identified multiple E3 ubiquitin ligases on the human lysosome membrane. Furthermore,
the ESCRT machinery was shown to be recruited to the human lysosome membrane.
In this proposed research, we plan to expand our initial findings by pursuing three specific aims.
Our Aim 1 will investigate how TORC1 regulates the vacuole membrane proteome via the
ubiquitin- and ESCRT-dependent pathway in yeast.
Our Aim 2 will study how yeast vacuole
membrane E3 ligases recognize their membrane substrates at both
structure and function levels.
Our Aim 3 will study how human lysosomes turnover their membrane proteins. Our research
will shed light on the development of new treatment strategies for LSDs and lysosome-
related neurodegenerative diseases.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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