Project 4: Capsid and nuclear import/integration co-factors
Project 4: Capsid and nuclear import/integration co-factors
批准号:
9977955
负责人:
Zandrea Ambrose
金额:
$41.33万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-27 至 2022-07-31
关键词:
Amino AcidsAreaBindingBiochemicalBiologyC-terminalCapsidCapsid ProteinsCell NucleusCellsCellular biologyCollaborationsComplexCryoelectron MicroscopyCrystallizationCytoplasmDependenceEventHIVHIV-1HumanImageImaging technologyInfectionIntegration Host FactorsKaryopherinsLabelLengthLife Cycle StagesLinkMediatingMediator of activation proteinMicrotubule-Organizing CenterMovementN-terminalNuclear ImportNuclear Pore Complex ProteinsPeptidesPlayPolyadenylationPrimate LentivirusesPrimatesProductionProteinsRecombinantsResolutionRoentgen RaysRoleSiteStructureTRIM GeneTimeTransport ProcessViralVirus ReplicationX-Ray CrystallographyZoonosescold temperaturenovelnucleocytoplasmic transportparticleprotein complexstructural biologytraffickingvirus host interaction
中文摘要
点击翻译按钮获取中文摘要
英文摘要
P4. Abstract
HIV-1 nuclear import is facilitated by the viral capsid protein (CA), interacting with several key cellular factors.
However, the precise roles of each of these interactions in the trafficking of the viral RTC/PIC toward the
nucleus and from the microtubule organizing center into the nucleus are poorly understood. We will utilize
advanced imaging technology and specifically labeled viral and cellular proteins to track CA and RTC/PIC
movements and interactions in real time, which will reveal hitherto unknown details of the early events of HIV-
1 biology that underlie viral trafficking, uncoating, nuclear import, and integration. We also will solve novel
structures of viral-host protein complexes that are involved in the nuclear transport process, including CA in
complex with NUP358, NUP153, and CPSF6 proteins, the latter also in complex with its β-karyopherin binding
partner TNPO3. The completion of Project 4 will yield novel information on the virus-host interactions that
underlie the key early events of the HIV-1 lifecycle at both the cell- and atomic levels.
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