以色列急性麻痹病毒LN株VP2蛋白序列分析及B淋巴细胞抗原表位预测
Sequence analysis and B lymphcyte antigenic epitope prediction of VP2 protein of Israeli acute paralysis virus LN strain
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摘要: 为分析以色列急性麻痹病毒(Israeli acute paralysis virus, IAPV)LN株VP2蛋白的序列并预测B淋巴细胞抗原表位,试验以IAPV-LN株RNA为模板,采用RT-PCR扩增VP2基因,通过BLAST序列比对获得IAPV-LN株VP2基因的核苷酸序列,并推导氨基酸序列,建立VP2蛋白的3D模型;用DNAStar软件中的Protean模块综合分析VP2蛋白的亲水性、柔性区域、表面可能性和抗原表位等。结果表明:IAPV-LN株VP2基因序列长度为810 bp,编辑了270个氨基酸,其与GenBank中公布的IAPV-BJ株(GenBank登录号为KX421583.1)核苷酸序列同源性为99%,氨基酸序列同源性为99%;与IAPV-BJ2(GenBank登录号为MG599488.1)株核苷酸序列同源性为98%,氨基酸序列同源性为99%。该蛋白是亲水性蛋白质,柔性区域和表面可能性区域较多;IAPV-LN株VP2蛋白空间构象比较规则,其可能形成抗原表位的区域是14~22,167~175,239~246位氨基酸处。Abstract: In order to analyze the sequence of VP2 protein of Israeli acute paralysis virus(IAPV) LN strain and to predict the B lymphcyte antigenic epitope, in the experiment, the IAPV-LN strain RNA was used as a template, the VP2 gene was amplified by RT-PCR,the nucleotide sequence of the IAPV-LN strain VP2 gene was obtained through BLAST sequence alignment, and the amino acid sequence was deduced to establish a 3 D model of the VP2 protein. The Protein module in DNAStar software was used to comprehensively analyze the hydrophilicity, flexible area, surface possibility and antigenic epitope of VP2 protein. The results showed that the VP2 gene sequence of the IAPV-LN strain was 810 bp in length and 270 amino acids had been edited, which had a nucleotide sequence homology of 99% with the IAPV-BJ strain published in GenBank(GenBank accession number KX421583.1),and the amino acid sequence homology was 99%;the nucleotide sequence homology with the IAPV-BJ2(GenBank accession number MG599488.1) strain was 98%,and the amino acid sequence homology was 99%. It was hydrophilie protein, flexible area and surface possibility were more. The spatial conformation of the VP2 protein of the IAPV-LN strain was relatively regular, and the regions where it may form an epitope were at amino acids 14-22,167-175,and 239-246.