Fernandez-Munoz R, Coca-Prados M, Hsu M T
J Virol. 1979 Feb;29(2):612-23. doi: 10.1128/JVI.29.2.612-623.1979.
A new method was developed for isolation of intracellular forms of simian virus 40 (SV40) nucleoprotein complexes from SV40-infected CV-1 cells late in the infectious cycle. In contrast to the Triton extraction method, which yields only a 60-70S complex, this new procedure yielded three forms of SV40 nucleoprotein complexes: complex I, complex II, and the nature virion (V). The three nucleoprotein complexes differed in physical as well as biochemical properties. Complex I, which is only a small portion of the total SV42 nucleoprotein complexes late during infection, was active in synthesizing both SV40-specific DNA and RNA. Pulse-labeling experiments suggest the following metabolic pathway: I leads to II leads to V. Conversion of complex I to II occurred shortly after the completion of SV40 DNA replication and resulted in the inactivation of the biosynthetic activities of I.
一种新方法被开发出来,用于在感染周期后期从感染猿猴病毒40(SV40)的CV-1细胞中分离细胞内形式的SV40核蛋白复合物。与仅产生60 - 70S复合物的Triton提取方法不同,这个新程序产生了三种形式的SV40核蛋白复合物:复合物I、复合物II和天然病毒体(V)。这三种核蛋白复合物在物理和生化特性上有所不同。复合物I在感染后期仅占总SV42核蛋白复合物的一小部分,它在合成SV40特异性DNA和RNA方面具有活性。脉冲标记实验表明了以下代谢途径:I导致II导致V。复合物I向II的转化在SV40 DNA复制完成后不久发生,并导致I的生物合成活性失活。