Clegg J C, Brzeski H, Kennedy S I
J Gen Virol. 1976 Sep;32(3):413-30. doi: 10.1099/0022-1317-32-3-413.
Two previously undescribed stable polypeptides (referred to as nsp 90 and nsp 63) appear in mammalian and avian cells infected with Semliki Forest virus. They are distinguishable from the virus structural proteins and their known precursors by their molecular weights and tryptic peptide maps, and are identical in size to two polypeptides found in purified preparations of virus-specific RNA polymerase. Data from pulse-chase experiments and from the use of inhibitors of proteolytic cleavage indicate that nsp 90 and nsp 63 are synthesized via a series of post-translational cleavages from three larger polypeptides, p200, p184 and p150. The labelling kinetics after synchronous initiation of protein synthesis are also consistent with the synthesis of nsp 90 and nsp 63 from a common initiation site, and show that nsp 63 is located close to this site. It is concluded that nsp 90 and nsp 63 are components of the virus-specific RNA polymerase, and are synthesized via a post-translational cleavage scheme entirely separate from that leading to the synthesis of the virus structural proteins.
两种先前未被描述的稳定多肽(称为nsp 90和nsp 63)出现在感染了Semliki森林病毒的哺乳动物和禽类细胞中。通过它们的分子量和胰蛋白酶肽图,可将它们与病毒结构蛋白及其已知前体区分开来,并且它们的大小与在病毒特异性RNA聚合酶的纯化制剂中发现的两种多肽相同。脉冲追踪实验的数据以及蛋白水解切割抑制剂的使用表明,nsp 90和nsp 63是通过从三种较大的多肽p200、p184和p150进行一系列翻译后切割而合成的。蛋白质合成同步起始后的标记动力学也与从共同起始位点合成nsp 90和nsp 63一致,并表明nsp 63位于该位点附近。得出的结论是,nsp 90和nsp 63是病毒特异性RNA聚合酶的组成部分,并且是通过与导致病毒结构蛋白合成完全不同的翻译后切割方案合成的。