Brewer G J, Singh M
J Gen Virol. 1982 May;60(Pt 1):135-46. doi: 10.1099/0022-1317-60-1-135.
Using two-dimensional gel electrophoresis, we have examined the proteins whose synthesis is stimulated in Alteromonas espejiana by infection with the membrane-containing bacteriophage PM2. In addition to four virus structural proteins, 11 non-structural proteins have been resolved and identified by their apparent isoelectric points and molecular weights. The relative rate of synthesis of each of the proteins was determined during the course of infection. Synthesis of the earliest proteins began around 10 min after infection. Synthesis of the virus structural proteins as a group did not begin until about 25 min after infection. In contrast to these structural proteins, the rate of synthesis of most of the non-structural virus proteins began to decline between 30 and 35 min after infection. This time preceded the onset of cell lysis marked by ion leakage (47 min); it corresponded to the beginning of packaging of virus DNA, removing that DNA from replication and transcription. Protein processing could not be demonstrated by pulse-chase labelling. These 15 proteins account for all of the coding capacity of the virus DNA. The virus origin of 14 of these proteins was established in an in vitro transcription-translation system programmed by PM2 DNA.
我们利用二维凝胶电泳技术,研究了在含膜噬菌体PM2感染埃氏交替单胞菌(Alteromonas espejiana)时,其合成被刺激的蛋白质。除了四种病毒结构蛋白外,还通过其表观等电点和分子量解析并鉴定出了11种非结构蛋白。在感染过程中测定了每种蛋白质的相对合成速率。最早的蛋白质合成在感染后约10分钟开始。作为一个整体,病毒结构蛋白的合成直到感染后约25分钟才开始。与这些结构蛋白不同,大多数非结构病毒蛋白的合成速率在感染后30至35分钟之间开始下降。这个时间早于以离子泄漏为标志的细胞裂解开始时间(47分钟);它对应于病毒DNA包装的开始,使该DNA脱离复制和转录。脉冲追踪标记法未能证明蛋白质加工过程。这15种蛋白质占病毒DNA的所有编码能力。其中14种蛋白质的病毒来源是在由PM2 DNA编程的体外转录-翻译系统中确定的。