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Development and characterization of monoclonal antibodies against the N-terminal domain of African swine fever virus structural protein, p54

机译:非洲猪瘟病毒结构蛋白N-末端结构域单克隆抗体的开发与表征,P54

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African swine fever virus (ASFV), a re-emerging DNA virus, causes a highly contagious disease for domestic pigs. It is running rife worldwide and threatening the global swine industry. Protein p54 is an attractive candidate for ASFV diagnostic and vaccine design. In this work, we designed a peptide to mimic the N-terminal domain (NTD) of ASFV p54 and pretested it with sera from ASFV-infected pigs. The peptide could be well recognized by the sera, implying that the NTD of p54 contained some potential linear B cell epitopes. Then, the conjugates of the peptide with bovine serum albumin were used as the immunogen to generate monoclonal antibodies (mAbs). A total of six mAbs specific to the NTD of ASFV p54 protein were developed. Five of them well reacted with ASFV HLJ/18 strain and recognized a same linear B cell epitope (5)FPZPV(9). Furthermore, epitope 'FFQPIP could be well recognized by ASFV-positive sera from natural infected pigs, suggesting that it was a natural linear B-cell epitope. Conservation analysis indicated that epitope (5)FFQPV(9) were highly conserved among ASFV epidemic isolates belonging to genotype I and II. Alanine-scanning mutagenesis further revealed that the residues (61 to 9V) of epitope (5)FFQPV(9) were the core binding sites for antibody recognition. This is the first research to characterize specific mAbs against NTD of p54 protein. These findings may help further understand the function of p54 protein and the improvement of ASFV diagnosis. (C) 2021 Elsevier B.V. All rights reserved.
机译:非洲猪瘟病毒(ASFV)是一种重新出现的DNA病毒,对家猪造成高度传染性疾病。它在全球范围内盛行,威胁着全球养猪业。p54蛋白是ASFV诊断和疫苗设计的一个有吸引力的候选蛋白。在这项工作中,我们设计了一种肽来模拟ASFV p54的N末端结构域(NTD),并用ASFV感染猪的血清对其进行了预测试。该肽可以被血清很好地识别,这意味着p54的NTD包含一些潜在的线性B细胞表位。然后,将肽与牛血清白蛋白的结合物用作免疫原,以产生单克隆抗体(MAB)。总共开发了六种特异于ASFV p54蛋白NTD的单克隆抗体。其中5株与ASFV HLJ/18株反应良好,识别出相同的线性B细胞表位(5)FPZPV(9)。此外,来自自然感染猪的ASFV阳性血清可以很好地识别表位FFQPIP,这表明它是一个自然的线性B细胞表位。保守分析表明,在属于基因型I和II的ASFV流行株中,表位(5)FFQPV(9)高度保守。丙氨酸扫描突变进一步揭示表位(5)FFQPV(9)的残基(61至9V)是抗体识别的核心结合位点。这是首次研究针对p54蛋白NTD的特异性单克隆抗体。这些发现可能有助于进一步了解p54蛋白的功能,提高ASFV的诊断水平。(c)2021爱思唯尔B.V.保留所有权利。

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