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DESCRIPTION (provided by applicant): Capsid proteins of papillomaviruses (PV) have evolved functional domains for the proper interaction between themselves, with PV viral nonstructural proteins, with PV genomic DNA, and with host cell factors, allowing for morphogenesis of infectious viral particles. Analyses performed using virus-like particles (VLPs) and pseudoviruses as an endpoint for viral morphogenesis may or may not equate to the authentic virus propagated in differentiating host tissue. Our organotypic virus culture system, capable of supporting the complete viral life cycle, coupled with our expertise in using MAbs to study capsid conformation, place us in the unique position to initiate the first studies to directly compare VLP self-assembly with authentic PV synthesis. These studies will directly investigate a functional role for L2 protein in authentic virus morphogenesis and include investigating the role of L2 in the process of VLP self-assembly. Our studies will focus on 2 main genetic approaches. One will use a chimeric genetic approach allowing investigations to begin by looking for type-specific differences between large domains of the interacting proteins of 2 viral types. The other is to specifically mutate domains that have been alluded to by other laboratories as having a function related to virion morphogenesis. To accomplish our research goals we have developed four specific aims: (1) Investigate papillomavirus type-specific structural gene interactions; (2) Compare the genetic requirements for the assembly of virus-like particles (VLPs) to authentic virion morphogenesis; (3) Genetically analyze the role of capsid protein cysteine residues in virion morphogenesis; and (4) Investigate the role of the N-terminus of the L1 capsid protein in virion morphogenesis by mutational analyses. When completed the studies proposed will for the first time provide new insight into the molecular mechanisms of virion morphogenesis in a system capable of reproducing the natural complex processes of PV morphogenesis and infection in a differentiating environment.
期刊论文(17)
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会议论文
DOI: 10.1371/journal.pone.0017848
发表时间: 2011-03-14
期刊: PloS one
影响因子: 3.7
作者: [Karim R, Meyers C, Backendorf C, Ludigs K, Offringa R, van Ommen GJ, Melief CJ, van der Burg SH, Boer JM]
通讯作者: Boer JM
DOI: 10.1371/journal.ppat.1003384
发表时间: 2013
期刊: PLoS pathogens
影响因子: 6.7
作者: [Karim R, Tummers B, Meyers C, Biryukov JL, Alam S, Backendorf C, Jha V, Offringa R, van Ommen GJ, Melief CJ, Guardavaccaro D, Boer JM, van der Burg SH]
通讯作者: van der Burg SH
DOI: 10.3390/v7082823
发表时间: 2015-08-04
期刊: Viruses
影响因子: --
作者: [Biryukov J, Meyers C]
通讯作者: Meyers C
DOI: 10.1002/ijc.25800
发表时间: 2011-09-15
期刊: INTERNATIONAL JOURNAL OF CANCER
影响因子: 6.4
作者: [Wang, Xiaohong, Meyers, Craig, Guo, Ming, Zheng, Zhi-Ming]
通讯作者: Zheng, Zhi-Ming
9
    Understanding the Role of HAART in the Progression of HPV-Associated Oral Cancer
    Understanding the Role of HAART in the Progression of HPV-Associated Oral Cancer
    Effect of HPV16 and ART on the Epigenome Leading to AIDS-Associated Oral Cancer
    Effect of HPV16 and ART on the Epigenome Leading to AIDS-Associated Oral Cancer
    国内基金
    海外基金
    猪圆环病毒2型核衣壳(capsid)表面 Loops结构及其展示外源抗原表位的研究
    • 批准号:
      2018JJ2177
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2018
    • 负责人:
      王乃东
    • 依托单位: