Xing Junji, Liu Shengwang, Han Zongxi, Shao Yuhao, Li Huixin, Kong Xiangang
Division of Avian Infectious Diseases, National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, The Chinese Academy of Agricultural Sciences, Harbin, PR China.
J Microbiol. 2009 Oct;47(5):589-99. doi: 10.1007/s12275-009-0104-z. Epub 2009 Oct 24.
This report describes the identification of a novel linear B-cell epitope at the C-terminus of the membrane (M) protein of avian infectious bronchitis virus (IBV). A monoclonal antibody (MAb) (designated as 15E2) against the IBV M protein was prepared and a series of 14 partially-overlapping fragments of the IBV M gene were expressed with a GST tag. These peptides were subjected to enzyme-linked immunosorbent assay (ELISA) and western blotting analysis using MAb 15E2 to identify the epitope. A linear motif, (199)FATFVYAK(206), which was located at the C-terminus of the M protein, was identified by MAb 15E2. ELISA and western blotting also showed that this epitope could be recognized by IBV-positive serum from chicken. Given that 15E2 showed reactivity with the (199)FATFVYAK(206) motif, expressed as a GST fusion protein, in both western blotting and in an ELISA, we proposed that this motif represented a linear B-cell epitope of the M protein. The (199)FATFVYAK(206) motif was the minimal requirement for reactivity as demonstrated by analysis of the reactivity of 15E2 with several truncated peptides that were derived from the motif. Alignment and comparison of the 15E2-defined epitope sequence with the sequences of other corona-viruses indicated that the epitope is well conserved among chicken and turkey coronaviruses. The identified epitope should be useful in clinical applications and as a tool for the further study of the structure and function of the M protein of IBV.
本报告描述了在禽传染性支气管炎病毒(IBV)膜(M)蛋白C端鉴定出一个新的线性B细胞表位。制备了一种针对IBV M蛋白的单克隆抗体(MAb)(命名为15E2),并表达了一系列14个部分重叠的IBV M基因片段,带有GST标签。使用MAb 15E2对这些肽进行酶联免疫吸附测定(ELISA)和蛋白质印迹分析以鉴定表位。MAb 15E2鉴定出一个位于M蛋白C端的线性基序(199)FATFVYAK(206)。ELISA和蛋白质印迹还表明,该表位可被鸡的IBV阳性血清识别。鉴于15E2在蛋白质印迹和ELISA中均与以GST融合蛋白形式表达的(199)FATFVYAK(206)基序发生反应,我们认为该基序代表M蛋白的一个线性B细胞表位。如通过分析15E2与源自该基序的几个截短肽的反应性所证明,(199)FATFVYAK(206)基序是反应性的最低要求。将15E2定义的表位序列与其他冠状病毒的序列进行比对和比较表明,该表位在鸡和火鸡冠状病毒中高度保守。鉴定出的表位在临床应用中应有用,并且可作为进一步研究IBV M蛋白结构和功能的工具。