HIGH-THROUGHPUT ASSAY FOR INHIBITORS OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR-ASSOCIATED TYROSINE KINASE

被引:15
作者
KING, IC
FENG, M
CATINO, JJ
机构
[1] Schering-Plough Research Institute, Kenilworth, NJ 07033
关键词
D O I
10.1016/0024-3205(93)90619-E
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We have developed a colorimetric assay for the examination of inhibitors of epidermal growth factor (EGF) receptor-associated tyrosine kinase in intact cells. EGF receptor from cells treated with inhibitors is captured by an anti-EGF receptor antibody and the phosphotyrosine content is measured by an anti-phosphotyrosine antibody. The quantitative assay does not use radioactive substances and is configured for a high-throughput format. Since it is performed in intact cells, substances lower the phosphotyrosine content on the receptor by different mechanisms will be identified. One distinct feature of the assay is that it uses the natural substrate inside the cell as compared to others using artificial substrates in an unphysiological environment. This assay is easy to perform, is reproducible, and is compatible with many organic solvents and tissue culture media. Thus, it is useful for the discovery of EGF receptor kinase inhibitors from natural products or synthetic compounds and is particularly suitable for large-scale screening.
引用
收藏
页码:1465 / 1472
页数:8
相关论文
共 17 条
[11]  
KING CS, 1986, J BIOL CHEM, V261, P73
[12]   MECHANISMS OF ACTION IN NIH-3T3 CELLS OF GENISTEIN, AN INHIBITOR OF EGF RECEPTOR TYROSINE KINASE-ACTIVITY [J].
LINASSIER, C ;
PIERRE, M ;
LEPECQ, JB ;
PIERRE, J .
BIOCHEMICAL PHARMACOLOGY, 1990, 39 (01) :187-193
[13]  
MATSUI H, 1991, CANCER RES, V51, P6170
[14]  
RO J, 1988, CANCER RES, V48, P161
[15]   PROTEIN-KINASE ASSAY BY PAPER TRICHLOROACETIC-ACID METHOD - HIGH-PERFORMANCE USING PHOSPHOCELLULOSE PAPER AND WASHING AN ENSEMBLE OF SAMPLES ON FLAT SHEETS [J].
SAHAL, D ;
FUJITAYAMAGUCHI, Y .
ANALYTICAL BIOCHEMISTRY, 1987, 167 (01) :23-30
[16]  
SEO MK, 1988, CANCER RES, V48, P792
[17]  
STOSCHECK CM, 1986, CANCER RES, V46, P1030