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禽肉瘤病毒gag前体多肽在哺乳动物细胞中不被加工。

Avian sarcoma virus gag precursor polypeptide is not processed in mammalian cells.

作者信息

Vogt V M, Bruckenstein D A, Bell A P

出版信息

J Virol. 1982 Nov;44(2):725-30. doi: 10.1128/JVI.44.2.725-730.1982.

Abstract

We studied intracellular avian gag proteins (internal structural proteins of virions) in several mammalian cell lines transformed by Rous sarcoma virus. All lines examined contain gag antigens as determined by radioimmune assay. We used the techniques of protein blotting from polyacrylamide gels, which detects nanogram quantities of viral protein, to investigate the size of intracellular viral polypeptides. All of the lines that contained enough viral protein to be amenable to this type of analysis synthesized Pr76, the avian sarcoma virus gag precursor polypeptide, but failed to process it into mature virion proteins. In some cell lines, the recovery of Pr76 was greatly enhanced by the addition of a mixture of protease inhibitors, including the sulfhydryl-blocking reagent N-ethylmaleimide, to the lysis buffer. At least several of the mammalian cells also synthesized a viral polypeptide the size of Pr180, the precursor to reverse transcriptase. Since Rous sarcoma virus does not replicate or replicates extremely poorly in mammalian cells, the lack of processing suggests that cleavage and virion assembly are invariably associated.

摘要

我们研究了在劳斯肉瘤病毒转化的几种哺乳动物细胞系中的细胞内禽源gag蛋白(病毒粒子的内部结构蛋白)。通过放射免疫测定法确定,所有检测的细胞系均含有gag抗原。我们使用聚丙烯酰胺凝胶蛋白印迹技术(该技术可检测纳克量的病毒蛋白)来研究细胞内病毒多肽的大小。所有含有足够病毒蛋白以适合进行此类分析的细胞系均合成了Pr76,即禽肉瘤病毒gag前体多肽,但未能将其加工成成熟的病毒粒子蛋白。在一些细胞系中,通过向裂解缓冲液中添加蛋白酶抑制剂混合物(包括巯基封闭试剂N-乙基马来酰亚胺),Pr76的回收率大大提高。至少有几种哺乳动物细胞还合成了一种大小为Pr180(逆转录酶前体)的病毒多肽。由于劳斯肉瘤病毒在哺乳动物细胞中不复制或复制极差,缺乏加工表明切割和病毒粒子组装总是相关的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/facc/256320/43207eaced86/jvirol00152-0310-a.jpg

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