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利用噬菌体展示技术分析鉴定轮状病毒 A 非结构蛋白 NSP2 的抗体结合表位。

Identification of an antibody-binding epitope on the rotavirus A non-structural protein NSP2 using phage display analysis.

机构信息

Department of Microbiology, La Trobe University, Bundoora, Victoria 3083, Australia.

Enteric Virus Group, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria 3052, Australia.

出版信息

J Gen Virol. 2011 Oct;92(Pt 10):2374-2382. doi: 10.1099/vir.0.032599-0. Epub 2011 Jun 22.

Abstract

The non-structural protein 2 (NSP2) of rotavirus has important roles in rotavirus replication associated with RNA binding, hydrolysis of NTPs and RNA, and helix destabilizing properties. A cell-culture assay using an NSP2-specific mAb and polyclonal antiserum to block virus replication showed a 73 and 96 % reduction in the amount of virus produced during replication, respectively. Phage display technology was used to identify the antibody-binding region on the NSP2 protein with the motif (244)T-(Y/F)-Ø-Ø-Ø-X-K-Ø-G(252), where Ø is a hydrophilic residue and X is any amino acid. This region was mapped to the three-dimensional NSP2 crystal structure to visualize the epitope. Analysis revealed identity to a region on NSP2 that mapped to a site exposed on the surface of the protein, which could possibly interfere with a functionally important region of the protein. Antibody binding to this region could disrupt the essential roles of NSP2, such as the formation of viroplasms with NSP5 or the interaction with viral RNA, thereby indicating a possible mechanism for the observed inhibition of virus replication. Genetic analysis of the putative binding region of NSP2 revealed a high level of conservation, suggesting that the region is under strict control.

摘要

轮状病毒的非结构蛋白 2(NSP2)在与 RNA 结合、NTP 和 RNA 水解以及螺旋不稳定特性相关的轮状病毒复制中具有重要作用。使用 NSP2 特异性 mAb 和多克隆抗血清阻断病毒复制的细胞培养测定显示,病毒复制过程中产生的病毒量分别减少了 73%和 96%。噬菌体展示技术用于鉴定 NSP2 蛋白上与基序 (244)T-(Y/F)-Ø-Ø-Ø-X-K-Ø-G(252)结合的抗体结合区域,其中Ø是亲水性残基,X 是任何氨基酸。该区域映射到 NSP2 的三维晶体结构以可视化表位。分析表明,它与 NSP2 上的一个区域具有同一性,该区域映射到蛋白质表面上暴露的位点,该位点可能干扰蛋白质的功能重要区域。抗体与该区域的结合可能会破坏 NSP2 的基本作用,例如与 NSP5 形成类病毒体或与病毒 RNA 的相互作用,从而表明观察到的病毒复制抑制的可能机制。NSP2 假定结合区域的遗传分析显示出高度的保守性,表明该区域受到严格控制。

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