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禽舍病毒粒子的重组:一个用于研究结构与组装的模型系统

Reconstitution of Flock House provirions: a model system for studying structure and assembly.

作者信息

Schneemann A, Gallagher T M, Rueckert R R

机构信息

Institute for Molecular Virology, College of Agricultural and Life Sciences, University of Wisconsin, Madison 53706.

出版信息

J Virol. 1994 Jul;68(7):4547-56. doi: 10.1128/JVI.68.7.4547-4556.1994.

Abstract

Assembly of Flock House virus in infected Drosophila cells proceeds through an intermediate, the provirion, which lacks infectivity until the coat precursor protein, alpha, undergoes a spontaneous "maturation" cleavage (A. Schneemann, W. Zhong, T. M. Gallagher, and R. R. Rueckert, J. Virol 6:6728, 1992). We describe here methods for purifying provirions in a state which permitted dissociation and reassembly. Dissociation, to monomeric alpha protein and free RNA, was accomplished by freezing at pH 9.0 in the presence of 0.5 M salt and 0.1 M urea. When dialyzed at low ionic strength and pH 6.5, the dissociation products reassembled spontaneously to form homogeneous provirions with a normal complement of RNA as judged by cosedimentation with authentic virions and by ability to undergo maturation cleavage with acquisition of substantial, though subnormal, infectivity. Reconstitution experiments, i.e., remixing components after separating RNA from capsid protein, generated abnormal particles, suggesting the presence in the unfractionated dissociation products of an unidentified "nucleating" component.

摘要

禽病毒在受感染的果蝇细胞中组装通过一种中间体——前病毒粒子进行,前病毒粒子直到衣壳前体蛋白α经历自发的“成熟”切割才具有感染性(A. Schneemann、W. Zhong、T. M. Gallagher和R. R. Rueckert,《病毒学杂志》6:6728,1992年)。我们在此描述了以允许解离和重新组装的状态纯化前病毒粒子的方法。通过在0.5 M盐和0.1 M尿素存在下于pH 9.0冷冻实现解离为单体α蛋白和游离RNA。当在低离子强度和pH 6.5下透析时,解离产物自发重新组装形成均匀的前病毒粒子,其具有正常的RNA互补物,这通过与真实病毒粒子的共沉降以及通过经历成熟切割并获得大量(尽管低于正常水平)感染性的能力来判断。重组实验,即在将RNA与衣壳蛋白分离后重新混合各组分,产生了异常颗粒,这表明在未分级的解离产物中存在一种未鉴定的“成核”组分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6377/236381/f6b03b5afcba/jvirol00016-0456-a.jpg

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