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Role of cdks and dynein in HCMV Assembly

Role of cdks and dynein in HCMV Assembly
cdks 和动力蛋白在 HCMV 组装中的作用
批准号:
7078623
负责人:
VERONICA SANCHEZ
金额:
$10.79万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-07-18 至 2007-02-28

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中文摘要
翻译
描述(由申请人提供):本申请的目的是为维罗妮卡·桑切斯博士作为疱疹病毒学领域的研究科学家的培训提供持续的支持。拟议工作的第一阶段将在加州大学圣地亚哥分校Deborah Spector博士的实验室指导环境中培养她的研究和教学技能。第二阶段将标志着她向学术界独立研究职位的过渡。
英文摘要
DESCRIPTION (provided by applicant): The goal of this application is to provide continuing support for Dr. Veronica Sanchez' training as a research scientist in the field of herpesvirology. Phase I of the proposed work will cultivate her research and teaching skills in a mentored environment in the laboratory of Dr. Deborah Spector at UCSD. Phase II will mark her transition to an independent research position in academia. Microtubule-based transport plays an important role in many cellular processes. Cytoplasmic dynein is a multimeric protein that, in association with the dynactin complex, mediates the transport of membranous and non-membranous cargo toward the microtubule-organizing center (MTOC) at the centrosome. Because the site of human cytomegalovirus (HCMV) envelopment overlaps the MTOC, we propose that dynein is involved in the transport of nucleocapsids from the nucleus to the cytoplasmic assembly compartment. To address this hypothesis, the expression and localization of dynein and dynactin subunits in HCMV-infected fibroblasts will be established. In addition, a functional analysis of dynein activity will be undertaken. Dynein activity will be inhibited in HCMV-infected cells by over-expression of dynactin subunits or small interfering RNAs (siRNAs) from recombinant viruses. The effects of dynein inhibition on the transport of nucleocapsids to the cytoplasmic assembly compartment will be determined by electron microscopy and immunofluorescence assays. The regulation of dynein activity by the cyclin-dependent kinases (cdks) in infected cells will also be studied. Recombinant HCMV viruses expressing dominant-negative forms of the cdks or siRNAs targeting the cyclins will be used to study the effect of phosphorylation on dynein activity in infected cells. These studies should provide valuable information regarding the role of dynein and cdk activity in HCMV assembly. In addition, the results from these studies will provide the basis for Dr. Sanchez to develop an independent research program and assist her to secure a faculty position at a university or medical school.
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Analysis of the macrophage membrane proteome: effects of viral infection
Analysis of the macrophage membrane proteome: effects of viral infection
Role of cdks and dynein in HCMV Assembly
Role of cdks and dynein in HCMV Assembly
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