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一种单克隆抗体可识别H6N1禽流感病毒血凝素上一个高度保守的中和表位。

A monoclonal antibody recognizes a highly conserved neutralizing epitope on hemagglutinin of H6N1 avian influenza virus.

作者信息

He Jie-Long, Hsieh Ming-Shou, Juang Rong-Huay, Wang Ching-Ho

机构信息

Department of Biochemical Science and Technology, Institute of Microbiology and Biochemistry, National Taiwan University, Taipei, Taiwan.

Department of Biochemical Science and Technology, Institute of Microbiology and Biochemistry, National Taiwan University, Taipei, Taiwan.

出版信息

Vet Microbiol. 2014 Dec 5;174(3-4):333-341. doi: 10.1016/j.vetmic.2014.10.008. Epub 2014 Oct 25.

Abstract

Neutralizing antibodies on the globular head of the hemagglutinin (HA) of avian influenza virus (AIV) are crucial for controlling this disease. However, most neutralizing antibodies lack cross reaction. This report describes the identification of a hemagglutinin epitope on the globular head near the receptor binding site of the H6N1 AIV. A monoclonal antibody named EB2 was prepared against the H6N1 AIV HA. Flow cytometry of AIV-infected chicken embryo fibroblast, DF-1 cells and specific-pathogen-free embryonated eggs were used to verify the neutralizing activity of this mAb. To narrow down the binding region, partially overlapping HA fragments and synthetic peptides were used to map the epitope by immune-blotting. The linear motif RYVRMGTESMN, located on the surface on the globular head of the HA protein, was identified as the epitope bound by EB2 mAb. Alignment of the EB2-defined epitope with other H6 AIVs showed that this epitope was conserved and specific to H6. We propose that this motif is a linear B-cell epitope of the HA protein and is near the receptor binding site. The identified epitope might be useful for clinical applications and as a tool for further study of the structure and function of the AIV HA protein.

摘要

禽流感病毒(AIV)血凝素(HA)球状头部的中和抗体对于控制该疾病至关重要。然而,大多数中和抗体缺乏交叉反应。本报告描述了在H6N1 AIV受体结合位点附近球状头部鉴定出的一个血凝素表位。制备了一种针对H6N1 AIV HA的单克隆抗体,命名为EB2。使用感染AIV的鸡胚成纤维细胞、DF-1细胞和无特定病原体的受精蛋进行流式细胞术,以验证该单克隆抗体的中和活性。为了缩小结合区域,使用部分重叠的HA片段和合成肽通过免疫印迹来定位表位。位于HA蛋白球状头部表面的线性基序RYVRMGTESMN被鉴定为EB2单克隆抗体结合的表位。将EB2定义的表位与其他H6 AIV进行比对,结果表明该表位是保守的且对H6具有特异性。我们提出该基序是HA蛋白的线性B细胞表位,且靠近受体结合位点。所鉴定的表位可能对临床应用有用,并可作为进一步研究AIV HA蛋白结构和功能的工具。

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