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由Sf9细胞合成的人α2HS-糖蛋白的分离。

Isolation of human alpha 2HS-glycoprotein synthesized by Sf9 cells.

作者信息

Lörincz Z, Kalabay L, Cseh S, Závodszky P, Arnaud P, Jakab L

机构信息

Institute of Enzymology, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Acta Microbiol Immunol Hung. 1998;45(3-4):419-24.

PMID:9873947
Abstract

The human alpha 2HS-glycoprotein is a negative acute phase protein synthesized by hepatocytes. Because of its fragility and the difficulty of its purification, we used recombinant DNA techniques to produce the protein in order to investigate its biological effects. The cDNA coding for the whole alpha 2HS-glycoprotein from human liver library had been cloned into the baculovirus expression vector system using the pVL 1392 transfer vector and Sf9 cells. The recombinant protein was synthesized in the Sf9 cells and was isolated on a hydroxiapatite column from the culture medium. Western blot analysis indicated that the cells synthesized large quantities of the recombinant human protein. The molecular mass of the recombinant AHSG was the same as that of the protein in human plasma but was slightly lower than that of AHSG in the cell culture supernatants of HepG2 and higher than that of AHSG from Hep3B cell cultures, respectively.

摘要

人α2HS - 糖蛋白是一种由肝细胞合成的负急性期蛋白。由于其易碎性以及纯化困难,我们利用重组DNA技术来生产该蛋白,以便研究其生物学效应。编码来自人肝脏文库的完整α2HS - 糖蛋白的cDNA已使用pVL 1392转移载体和Sf9细胞克隆到杆状病毒表达载体系统中。重组蛋白在Sf9细胞中合成,并从培养基中在羟基磷灰石柱上分离出来。蛋白质免疫印迹分析表明细胞合成了大量的重组人蛋白。重组AHSG的分子量与人血浆中的蛋白相同,但分别略低于HepG2细胞培养上清液中的AHSG,且高于Hep3B细胞培养物中的AHSG。

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