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使用放线菌酮预处理增强病毒蛋白合成来检测2型腺病毒诱导的早期多肽。

Detection of adenovirus type 2-induced early polypeptides using cycloheximide pretreatment to enhance viral protein synthesis.

作者信息

Harter M L, Shanmugam G, Wold W S, Green M

出版信息

J Virol. 1976 Jul;19(1):232-42. doi: 10.1128/JVI.19.1.232-242.1976.

Abstract

(35S) methionine-labeled polypeptides synthesized by adenovirus type 2-infected cells have been analyzed by polyacrylamide gradient gel electrophoresis and autoradiography. Cycloheximide (CH) was added to infected cultures to accumulate early viral mRNA relative to host cell mRNA. This allowed viral proteins to be synthesized in increased amounts relative to host proteins after removal of CH and pulse-labeling with (35S)methionine. During the labeling period arabinosyl cytosine was added to prevent the synthesis of late viral proteins. This procedure facilitated the detection of six early viral-induced polypeptides, designated EP1 through EP6 (early protein), with apparent molecular weights of 75,000 (75K), 42K, 21K, 18K, 15K, and 11K. Supportive data were obtained by coelectrophoresis of (35S)- and (3H)methionine-labeled polypeptides from infected and uninfected cells, respectively. Three of these early polypeptides have not been previously reported. CH pretreatment enhanced the rates of synthesis of EP4 and EP6 20- to 30-fold and enhanced that of the others approximately twofold. The maximal rates of synthesis of the virus-induced proteins varied, in a different manner, with time postinfection and CH pretreatment. Since CH pretreatment appears to increase the levels of early viral proteins, it may be a useful procedure to assist their isolation and functional characterization.

摘要

通过聚丙烯酰胺梯度凝胶电泳和放射自显影分析了腺病毒2型感染细胞合成的(35S)甲硫氨酸标记的多肽。向感染的培养物中加入放线菌酮(CH),以相对于宿主细胞mRNA积累早期病毒mRNA。这使得在去除CH并用(35S)甲硫氨酸进行脉冲标记后,相对于宿主蛋白,病毒蛋白能够以增加的量合成。在标记期间加入阿糖胞苷以防止晚期病毒蛋白的合成。该程序有助于检测六种早期病毒诱导的多肽,命名为EP1至EP6(早期蛋白),其表观分子量分别为75,000(75K)、42K、21K、18K、15K和11K。通过分别对来自感染和未感染细胞的(35S)和(3H)甲硫氨酸标记的多肽进行共电泳获得了支持性数据。这些早期多肽中的三种以前尚未见报道。CH预处理使EP4和EP6的合成速率提高了20至30倍,使其他多肽的合成速率提高了约两倍。病毒诱导蛋白的最大合成速率随感染后时间和CH预处理的方式不同而变化。由于CH预处理似乎增加了早期病毒蛋白的水平,它可能是有助于其分离和功能表征的有用程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc95/354851/02d533cf1f32/jvirol00223-0244-a.jpg

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