Jagadish M N, Staton V J, Hudson P J, Azad A A
CSIRO, Division of Protein Chemistry, Parkville, Australia.
J Virol. 1988 Mar;62(3):1084-7. doi: 10.1128/JVI.62.3.1084-1087.1988.
The cDNA fragment of the large RNA segment of infectious bursal disease virus 002-73, when expressed in Escherichia coli, produces precursor polyprotein (N-VP2-VP4-VP3-C), most of which is then processed to generate constituent polypeptides. Using cDNA fragments containing site-specific mutations and two monoclonal antibodies that are specific to VP2 and VP3 of mature virus particles, we demonstrated that the VP4 protein is involved in processing of the precursor polyprotein to generate VP2 and VP3 and excluded the possibility of internal initiation for the generation of VP3.
传染性法氏囊病病毒002 - 73大RNA片段的cDNA片段在大肠杆菌中表达时,会产生前体多聚蛋白(N - VP2 - VP4 - VP3 - C),随后大部分前体多聚蛋白会被加工以产生组成多肽。利用含有位点特异性突变的cDNA片段以及两种对成熟病毒颗粒的VP2和VP3具有特异性的单克隆抗体,我们证明VP4蛋白参与前体多聚蛋白的加工以产生VP2和VP3,并排除了VP3产生过程中内部起始的可能性。