Ng L F, Liu D X
Institute of Molecular Agrobiology, Singapore.
Virology. 1998 Apr 10;243(2):388-95. doi: 10.1006/viro.1998.9058.
We report here the identification of a 24-kDa polypeptide in IBV-infected Vero cells by immunoprecipitation with a region-specific antiserum raised in rabbits against the IBV sequence encoded between nucleotides 10,928 and 11,493. Coexpression, deletion, and mutagenesis studies have demonstrated that this protein is encoded by ORF 1a from nucleotide 10,915 to 11,544 and is released from the 1a polyprotein by the 3C-like proteinase-mediated proteolysis. A previously predicted Q-S (Q3462S3463) dipeptide bond encoded by the IBV sequence from nucleotide 10,912 to 10,917 is identified as the N-terminal cleavage site, and a Q-N (Q3672N3673) dipeptide bond encoded by the IBV sequence between nucleotides 11,542 and 11,547 is identified as the C-terminal cleavage site of the 24-kDa polypeptide.
我们在此报告,通过用兔体内产生的针对传染性支气管炎病毒(IBV)核苷酸10928至11493之间编码序列的区域特异性抗血清进行免疫沉淀,在感染IBV的非洲绿猴肾细胞(Vero细胞)中鉴定出一种24 kDa的多肽。共表达、缺失和诱变研究表明,该蛋白由核苷酸10915至11544的开放阅读框1a(ORF 1a)编码,并通过3C样蛋白酶介导的蛋白水解作用从1a多蛋白中释放出来。由IBV核苷酸10912至10917编码的先前预测的Q-S(Q3462S3463)二肽键被确定为N端切割位点,而由IBV核苷酸11542至11547之间编码的Q-N(Q3672N3673)二肽键被确定为24 kDa多肽的C端切割位点。