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日本脑炎病毒NS1蛋白上病毒特异性保守B细胞表位的鉴定

Identification of a virus-specific and conserved B-cell epitope on NS1 protein of Japanese encephalitis virus.

作者信息

Wang Bin, Hua Rong-Hong, Tian Zhi-Jun, Chen Na-Sha, Zhao Fu-Rong, Liu Tian-Qiang, Wang Yun-Feng, Tong Guang-Zhi

机构信息

National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 427 Maduan Street, Harbin 150001, Heilongjiang, China.

出版信息

Virus Res. 2009 Apr;141(1):90-5. doi: 10.1016/j.virusres.2009.01.004. Epub 2009 Jan 29.

Abstract

NS1 protein of Japanese encephalitis virus (JEV) is an important non-structural protein, which is able to induce protective immune response in target animals and can be used as specific serological diagnosis tool, but the epitopes on NS1 of JEV have not been identified. For epitope mapping, in this study, a series of 51 partially overlapping fragments covering entire NS1 protein were expressed with a GST-tag and then screened by a monoclonal antibody (mAb). Through enzyme-linked immunosorbent assay (ELISA), linear epitope-containing fragment, the overlapping region of NS1-18 and NS1-19 (residues 145-152), was located. Then a set of peptides derived from that overlapping region with deletions were expressed and subjected to ELISA and Western blot for further mapping purpose. Results indicated that the motif of (146)EHARW(150) is the minimal unit of the linear epitope recognized by that monoclonal antibody (mAb). Western blot showed that this epitope could be recognized by JEV-positive serum from pigs. Furthermore, it was found that the epitope is highly conserved among JEV strains through sequence alignments analysis. Notably, none of the homologous regions on NS1 proteins of other flavivirus could react with the mAb when they were tested for cross-reactivity, suggesting the potential clinical application of this epitope in differential diagnosis.

摘要

日本脑炎病毒(JEV)的NS1蛋白是一种重要的非结构蛋白,它能够在靶动物中诱导保护性免疫反应,并且可作为特异性血清学诊断工具,但JEV的NS1上的表位尚未得到鉴定。为了进行表位定位,在本研究中,一系列覆盖整个NS1蛋白的51个部分重叠片段用谷胱甘肽S-转移酶(GST)标签进行表达,然后用单克隆抗体(mAb)进行筛选。通过酶联免疫吸附测定(ELISA),定位到含线性表位的片段,即NS1-18和NS1-19的重叠区域(第145-152位氨基酸残基)。然后表达一组源自该重叠区域且有缺失的肽,并进行ELISA和蛋白质印迹以进一步进行表位定位。结果表明,(146)EHARW(150)基序是该单克隆抗体识别的线性表位的最小单位。蛋白质印迹显示该表位可被猪的JEV阳性血清识别。此外,通过序列比对分析发现该表位在JEV毒株中高度保守。值得注意的是,当测试其他黄病毒的NS1蛋白上的同源区域的交叉反应性时,它们均不能与该单克隆抗体发生反应,这表明该表位在鉴别诊断中具有潜在的临床应用价值。

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