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成人T细胞白血病病毒的前体多肽:用针对分离出的多肽gp68、p24和p19的抗血清进行检测。

Precursor polypeptides of adult T-cell leukaemia virus: detection with antisera against isolated polypeptides gp68, p24 and p19.

作者信息

Schneider J, Yamamoto N, Hinuma Y, Hunsmann G

出版信息

J Gen Virol. 1984 Dec;65 ( Pt 12):2249-58. doi: 10.1099/0022-1317-65-12-2249.

Abstract

Sera of individuals infected with adult T-cell leukaemia virus (ATLV) react predominantly with the polypeptides gp68, p24 and p19. These polypeptides were isolated from ATLV-infected MT-2 cells and virus. The radioiodinated polypeptides were used to quantify respective antibodies in individual ATLV carrier sera. Heteroantisera prepared in rabbits against isolated polypeptides facilitated studies on the biosynthesis of the core and envelope polypeptides of ATLV. Pulse-chase experiments revealed a polypeptide of mol. wt. 48 000 (48K) as the precursor to the core polypeptides p24 and p19. A 28K polypeptide related to p19 appeared to be an early side-product of the gag gene or a translate of a defective viral message. Antiserum to the putative env gene product gp68 recognized gp68, gp66 and small amounts of gp62. In tunicamycin-treated cells gp68, gp66 and gp62 were no longer synthesized, but a 54K polypeptide reacted with antiserum to gp68. Polypeptide p54 is structurally related to gp68 and therefore apparently represents the unglycosylated form of gp68. Moreover, the apparent mol. wt. of p54 and p48 agree with those predicted for respective env and gag precursors from the nucleotide sequence of an ATLV provirus.

摘要

感染成人T细胞白血病病毒(ATLV)的个体血清主要与多肽gp68、p24和p19发生反应。这些多肽是从感染ATLV的MT - 2细胞和病毒中分离出来的。用放射性碘标记的多肽来定量个体ATLV携带者血清中的相应抗体。用兔制备的针对分离多肽的异种抗血清有助于对ATLV核心和包膜多肽的生物合成进行研究。脉冲追踪实验显示,分子量为48000(48K)的一种多肽是核心多肽p24和p19的前体。一种与p19相关的28K多肽似乎是gag基因的早期副产物或有缺陷病毒信息的翻译产物。针对假定env基因产物gp68的抗血清识别gp68、gp66和少量的gp62。在衣霉素处理的细胞中,不再合成gp68、gp66和gp62,但一种54K多肽能与针对gp68的抗血清发生反应。多肽p54在结构上与gp68相关,因此显然代表gp68的未糖基化形式。此外,p54和p48的表观分子量与根据ATLV前病毒核苷酸序列预测的相应env和gag前体的分子量相符。

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