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腺病毒组装过程中的中间体。

Intermediates in adenovirus assembly.

作者信息

Edvardsson B, Everitt E, Jörnvall H, Prage L, Philipson L

出版信息

J Virol. 1976 Aug;19(2):533-47. doi: 10.1128/JVI.19.2.533-547.1976.

Abstract

Three intermediates in adenovirus assembly have been defined; nuclear intermediates, young virions, and mature virions. The nuclear intermediates are fragile and heterogenous in size (550S-670S) and withstand separation on ficoll gradients but fall apart upon CsCl gradient centrifugation unless prefixed with glutaraldehyde. They contain both capsid and core structures, and the core structures are preferentially released during purification in CsCl. The precursor polypeptides pVI and pVII are present in the intermediates without any corresponding mature polypeptide. The young virions (Ishibashi and Maizel, 1974) are stable and preferentially confined to the nuclei after cell fractionation. They contain both uncleaved precursor polypeptides and their cleavage products. The mature virions accumulate in the cytoplasm during cell fractionation and contain the final mature polypeptides. Pulse-chase labeling kinetics, focusing on the precursor polypeptides, suggest that these three classes participate in assembly of adenovirus. Tryptic peptide maps establish that polypeptide pVI is the precursor of polypeptide VI, but only a small fraction of polypeptide 26K can in vivo account for polypeptide VIII.

摘要

腺病毒组装过程中的三种中间体已被确定,即核中间体、年轻病毒体和成熟病毒体。核中间体很脆弱,大小不均一(550S - 670S),能在菲可梯度上耐受分离,但在氯化铯梯度离心时会解体,除非先用戊二醛固定。它们包含衣壳和核心结构,并且在氯化铯纯化过程中核心结构会优先释放。前体多肽pVI和pVII存在于中间体中,没有任何相应的成熟多肽。年轻病毒体(石桥和梅泽尔,1974年)很稳定,在细胞分级分离后优先局限于细胞核中。它们既包含未切割的前体多肽及其切割产物。成熟病毒体在细胞分级分离过程中积聚在细胞质中,并包含最终的成熟多肽。以这些前体多肽为重点的脉冲追踪标记动力学表明,这三类中间体参与了腺病毒的组装。胰蛋白酶肽图谱确定多肽pVI是多肽VI的前体,但在体内只有一小部分26K多肽能形成多肽VIII。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d90f/354890/2b4b294b65b3/jvirol00224-0256-a.jpg

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