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猫肉瘤病毒编码的多蛋白:由C型病毒编码的结构蛋白进行酶切裂解。

Feline sarcoma virus-coded polyprotein: enzymatic cleavage by a type C virus-coded structural protein.

作者信息

Khan A S, Stephenson J R

出版信息

J Virol. 1979 Feb;29(2):649-56. doi: 10.1128/JVI.29.2.649-656.1979.

Abstract

A purified 15,000-molecular-weight (Mr) Prague strain Rous sarcoma virus gag gene-coded structural protein, p15, was shown to enzymatically cleave the previously described 130,000 Mr feline sarcoma virus-coded polyprotein, Pr130. Cleavage products included proteins ranging in molecular weight from 12,000 to 110,000. The specificity of this cleavage reactivity was indicated by the fact that, under similar conditions, neither purified type C viral structural proteins nor nonviral proteins such as bovine serum albumin were cleaved to significant extents. Moreover, feline leukemia virus Pr65gag was efficiently cleaved, resulting in the generations of proteins of 30,000 (p30), 15,000 (p15), 12,000 (p12), and 10,000 (p10) Mr. Using enzymatically (p15) treated feline sarcoma virus Pr130 as starting material, we were able to purify a major 72,000 Mr cleavage product and to show it to contain the previously described feline sarcoma virus-coded nonstructural component.

摘要

一种纯化的分子量为15,000(Mr)的布拉格株劳氏肉瘤病毒gag基因编码的结构蛋白p15,被证明能酶解先前描述的分子量为130,000的猫肉瘤病毒编码的多蛋白Pr130。酶解产物包括分子量从12,000到110,000不等的蛋白质。这种酶解反应的特异性表现在,在相似条件下,纯化的C型病毒结构蛋白和非病毒蛋白如牛血清白蛋白都没有被显著酶解。此外,猫白血病病毒Pr65gag被有效酶解,产生了分子量为30,000(p30)、15,000(p15)、12,000(p12)和10,000(p10)的蛋白质。以经酶(p15)处理的猫肉瘤病毒Pr130为起始材料,我们能够纯化出一种主要的分子量为72,000的酶解产物,并证明它含有先前描述的猫肉瘤病毒编码的非结构成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d79d/353197/65264da2c911/jvirol00182-0239-a.jpg

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