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用伴刀豆球蛋白A亲和层析法分离单纯疱疹病毒诱导的抗原。

Separation of Herpes simplex virus-induced antigens by Concanavalin A affinity chromatography.

作者信息

Ponce de Leon M, Hessle H, Cohen G H

出版信息

J Virol. 1973 Oct;12(4):766-74. doi: 10.1128/JVI.12.4.766-774.1973.

Abstract

Biologically active herpes simplex virus (HSV)-induced antigens were selectively removed from extracts of infected BHK cells by affinity chromatography by utilizing an insoluble form of concanavalin A (Con A). Soluble extracts of (3)H-glucosamine-labeled, HSV-infected cells were absorbed to a Con A column. Bound material was eluted with alpha-methyl-d-mannoside (alphaMM) and NaCl. The specific activity of the eluted glycoproteins increased by 10-fold. Two broad groups of viral-induced antigens were isolated from Con A. Group I includes two antigens which bind to Con A by a specific mechanism because the antigens are dissociated by alphaMM. Group II contains three antigens which bind to Con A but apparently by a nonspecific or electrolytic mechanism. One antigen in group I was identified as the glycoprotein antigen, CP-1, described previously.

摘要

利用不溶性伴刀豆球蛋白A(Con A)通过亲和层析从感染的BHK细胞提取物中选择性去除具有生物活性的单纯疱疹病毒(HSV)诱导抗原。将用(3)H-葡萄糖胺标记的HSV感染细胞的可溶性提取物吸附到Con A柱上。结合的物质用α-甲基-D-甘露糖苷(αMM)和氯化钠洗脱。洗脱的糖蛋白的比活性提高了10倍。从Con A中分离出两大类病毒诱导抗原。第一组包括两种通过特定机制与Con A结合的抗原,因为这些抗原可被αMM解离。第二组包含三种与Con A结合但显然是通过非特异性或电解机制结合的抗原。第一组中的一种抗原被鉴定为先前描述的糖蛋白抗原CP-1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4411/356695/7a07b9a669b4/jvirol00262-0111-a.jpg

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