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猿猴病毒40小t抗原在大肠杆菌中的表达及抗原的纯化。

Expression of simian virus 40 small t antigen in Escherichia coli and purification of the antigen.

作者信息

Ikeda S, Akiyama K, Mitsunobu F, Wada T, Hatsushika M, Watanabe S, Tsutsui K, Seki S, Oda T

机构信息

Department of Biochemistry, Cancer Institute, Okayama University Medical School, Japan.

出版信息

Arch Geschwulstforsch. 1987;57(4):275-81.

PMID:2823739
Abstract

A simian virus 40 (SV 40) DNA fragment encoding small t antigen was cloned in expression vector pUC8 for the purification of the antigen. The SV40 Hind III B fragment was inserted into the Hind III site of pUC8. A plasmid having the lacZ' and small t antigen genes in the same orientation was designated as pSVt. pSVt encodes the entire small t antigen and an extra 18 amino acids at the amino terminus of the antigen. E. coli transformed with pSVt produced hybrid small t antigen (22 kDa) which comprised about 6% of the total protein. The hybrid small t antigen reacted in immunoblot analysis with SV40-induced tumor-bearing hamster serum. Hybrid small t antigen was extracted from E. coli, and purified by preparative SDS-PAGE. The antigen was extracted from the gel using formic acid solution with high-yield. The gel-purified antigen showed the same antigenic reactivity as crude antigen.

摘要

将编码小t抗原的猿猴病毒40(SV 40)DNA片段克隆到表达载体pUC8中,用于抗原的纯化。将SV40 Hind III B片段插入pUC8的Hind III位点。将具有同向lacZ'和小t抗原基因的质粒命名为pSVt。pSVt编码完整的小t抗原以及该抗原氨基末端额外的18个氨基酸。用pSVt转化的大肠杆菌产生杂合小t抗原(22 kDa),其约占总蛋白的6%。杂合小t抗原在免疫印迹分析中与SV40诱导的荷瘤仓鼠血清发生反应。从大肠杆菌中提取杂合小t抗原,并通过制备性SDS-PAGE进行纯化。使用甲酸溶液从凝胶中高效提取抗原。凝胶纯化的抗原与粗抗原具有相同的抗原反应性。

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