PURIFICATION AND CHARACTERIZATION OF SOLUBLE HUMAN IL-6 RECEPTOR EXPRESSED IN CHO CELLS

被引:163
作者
YASUKAWA, K
SAITO, T
FUKUNAGA, T
SEKIMORI, Y
KOISHIHARA, Y
FUKUI, H
OHSUGI, Y
MATSUDA, T
YAWATA, H
HIRANO, T
TAGA, T
KISHIMOTO, T
机构
[1] OSAKA UNIV,INST MOLEC & CELLULAR BIOL,SUITA,OSAKA 565,JAPAN
[2] TOSOH CORP,BIOTECHNOL RES LAB,AYASE,KANAGAWA 252,JAPAN
[3] OSAKA UNIV,SCH MED,BIOMED RES CTR,KITA KU,OSAKA 530,JAPAN
[4] CHUGAI PHARMACEUT CO LTD,FUJI GOTEMBA RES LABS,GOTEMBA,SHIZUOKA 412,JAPAN
关键词
D O I
10.1093/oxfordjournals.jbchem.a123261
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An immunosorbent assay system to detect genetically engineered IL-6 receptor (IL-6R) was established, whereby soluble IL-6 receptor (sEL-6R) was detected in the culture medium when sIL-6R cDNA was transfected into COS1cells. A stably transformed Chinese hamster ovary (CHO) cell line constitutively expressing sIL-6R has been established. The recom-binant sIL-6R was purified to homogeneity by sequential filtration and chromatography of the culture medium. The recombinant aIL-6R augmented the sensitivity of Ml cells to IL-6 in growth inhibition assay in a dose-dependent manner. Furthermore, a radioisotope immunosorbent assay (RIA) utilizing recombinant sIL-6R was established which could detect IL-6 in a quantity as low as 10 ng/ml. © 1990 Copyright, 1990 by the Journal of Biochemistry.
引用
收藏
页码:673 / 676
页数:4
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