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一种由双链RNA噬菌体phi 6的L片段编码的新的低丰度小非结构蛋白。

A new small low-abundant nonstructural protein encoded by the L segment of the dsRNA bacteriophage phi 6.

作者信息

Casini G, Revel H R

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, Illinois 60637.

出版信息

Virology. 1994 Sep;203(2):221-8. doi: 10.1006/viro.1994.1479.

Abstract

A new small low-abundant protein encoded by the large genome segment of bacteriophage phi 6 has been detected in extracts of Escherichia coli bearing phi 6 cDNA clones and in extracts of phage-infected Pseudomonas phaseolicola. This 62 amino acid protein, designated P14, has a net charge of +2 at pH 7.0. Gene 14 has been located by deletion analysis and N-terminal protein sequence. Expression of P14 is down-regulated in E. coli when the complete L segment clone is expressed. Polyclonal antibodies to P14 detected the new protein in small amounts in phage-infected cells but not in phi 6 virions or nucleocapsids, or in procapsids assembled in E. coli. Procapsids assembled in E. coli after expression of phi 6 L segment clones with or without gene 14 had essentially similar protein composition and activity in an in vitro packaging and replication system. Thus P14 does not appear to be essential for the structure or assembly of functional procapsids. P14 might, however, facilitate packaging in vivo. Alternatively this protein could play in a role in repair of host membranes following viral penetration.

摘要

在携带噬菌体φ6 cDNA克隆的大肠杆菌提取物以及噬菌体感染的菜豆假单胞菌提取物中,检测到了一种由噬菌体φ6大基因组片段编码的新的低丰度小蛋白。这种含有62个氨基酸的蛋白被命名为P14,在pH 7.0时净电荷为+2。通过缺失分析和N端蛋白序列确定了基因14的位置。当完整的L片段克隆表达时,大肠杆菌中P14的表达被下调。针对P14的多克隆抗体在噬菌体感染的细胞中检测到少量新蛋白,但在φ6病毒粒子、核衣壳或在大肠杆菌中组装的原衣壳中未检测到。在表达了含或不含基因14的φ6 L片段克隆后,在大肠杆菌中组装的原衣壳在体外包装和复制系统中具有基本相似的蛋白质组成和活性。因此,P14似乎对功能性原衣壳的结构或组装不是必需的。然而,P14可能有助于体内包装。或者,这种蛋白可能在病毒穿透后宿主膜的修复中发挥作用。

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