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16型腺病毒不完全颗粒的结构多肽

Structural polypeptides of adenovirus type 16 incomplete particles.

作者信息

Winberg G, Wadell G

出版信息

J Virol. 1977 May;22(2):389-401. doi: 10.1128/JVI.22.2.389-401.1977.

DOI:10.1128/JVI.22.2.389-401.1977
PMID:864832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC515730/
Abstract

The polypeptides of adenovirus type 16 incomplete particles, with average buoyant densities of CsCl of 1.33, 1.318, 1.305, and 1.299 g/cm3 and DNA content of less than 1 U genome size, were compared with the polypeptides of the complete virion (density, 1.344 g/cm3, and 22 x 10(6) daltons of DNA) and late polypeptides in infected cells by using sodium dodecyl sulfate-gel electrophoresis. In agreement with other serotypes studied (types 2 and 3), the light particles lack polypeptides V, VI, and VII. In adenovirus type 16, eight other major polypeptides are found, with apparent molecular weights of 59,000 (59K), 46K, 31K, 30K, 28K, 27K, 26K, and 19K. The 30K to 31K and 27K to 28K polypeptides are phosphorylated. The 27K and 19K polypeptides are precursors, whereas the 31K, 30K, and 26K polypeptides are chase products in the cell, as are polypeptides VI, VII, and VIII. The 26K polypeptide is proposed to be an intermediate in processing since it disappears from the young virions upon chasing. Although chase products, the 31K and 30K polypeptides are only associated with particles having buoyant density lower than 1.318 g/cm3. Polypeptides V and VII are only present in particles containing more than one quarter of the genome. No trace of cell histones could be detected in the purified incomplete particles. A major constituent of the incomplete particles, the 46K polypeptide, was rapidly labeled in the cell, and loss of radioactivity from this band was detectable only after 7 to 18 h of chase.

摘要

采用十二烷基硫酸钠 - 凝胶电泳法,将16型腺病毒不完全颗粒的多肽(氯化铯平均浮力密度分别为1.33、1.318、1.305和1.299 g/cm³,DNA含量小于1个基因组大小)与完整病毒体的多肽(密度为1.344 g/cm³,DNA为22×10⁶道尔顿)以及感染细胞中的晚期多肽进行了比较。与其他已研究的血清型(2型和3型)一致,轻颗粒缺乏多肽V、VI和VII。在16型腺病毒中,还发现了其他8种主要多肽,其表观分子量分别为59000(59K)、46K、31K、30K、28K、27K、26K和19K。30K至31K以及27K至28K的多肽被磷酸化。27K和19K的多肽是前体,而31K、30K和26K的多肽是细胞中的追踪产物,多肽VI、VII和VIII也是如此。26K多肽被认为是加工过程中的中间体,因为在追踪时它会从年轻病毒体中消失。虽然是追踪产物,但31K和30K多肽仅与浮力密度低于1.318 g/cm³的颗粒相关。多肽V和VII仅存在于基因组含量超过四分之一的颗粒中。在纯化的不完全颗粒中未检测到细胞组蛋白的痕迹。不完全颗粒的主要成分46K多肽在细胞中被快速标记,只有在追踪7至18小时后才能检测到该条带放射性的损失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/797a7776ab0f/jvirol00209-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/c95bdbf2264f/jvirol00209-0164-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/3a757da0ac0a/jvirol00209-0165-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/e1fb2b756c62/jvirol00209-0166-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/d0b33afdab09/jvirol00209-0167-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/17588db05928/jvirol00209-0168-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/797a7776ab0f/jvirol00209-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/c95bdbf2264f/jvirol00209-0164-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/3a757da0ac0a/jvirol00209-0165-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/e1fb2b756c62/jvirol00209-0166-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/d0b33afdab09/jvirol00209-0167-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/17588db05928/jvirol00209-0168-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b67/515730/797a7776ab0f/jvirol00209-0169-a.jpg

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