Screening for topoisomerase I binding compounds by high-performance liquid chromatography-mass spectrometry

被引:13
作者
Zhang, H
Gu, Q
Liang, XL
Pan, YJ [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou, Peoples R China
[2] Hangzhou Univ Commerce, Dept Food Sci, Hangzhou, Peoples R China
[3] Zhejiang Univ, Dept Biol, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1016/j.ab.2004.03.057
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new rapid compound screening approach for topoisomerase I binding activity is presented. DNA topoisomerase I is used as a target protein to capture binding compounds from a mixture of combinatorial compounds by bioaffinity ultrafiltration. Using high-performance liquid chromatography combined with electrospray ionization mass spectrometry, small-molecule active compounds were identified. We also have successfully applied this method to identifying compounds from cells grown in culture. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:173 / 179
页数:7
相关论文
共 14 条
[1]  
FENG JC, 2000, FORESTRY SCI, V36, P100
[2]   APPLICATIONS OF COMBINATORIAL TECHNOLOGIES TO DRUG DISCOVERY .1. BACKGROUND AND PEPTIDE COMBINATORIAL LIBRARIES [J].
GALLOP, MA ;
BARRETT, RW ;
DOWER, WJ ;
FODOR, SPA ;
GORDON, EM .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (09) :1233-1251
[3]   QUANTITATIVE-ANALYSIS OF SCHIZOPHYLLUM-COMMUNE METALLOPROTEASE SCPRB ACTIVITY IN SDS-GELATIN PAGE REVEALS DIFFERENTIAL MYCELIAL LOCALIZATION OF NITROGEN LIMITATION-INDUCED AUTOLYSIS [J].
GORDON, LJ ;
LILLY, WW .
CURRENT MICROBIOLOGY, 1995, 30 (06) :337-343
[4]  
Hengel A. J. V., 1992, PLANT CELL TISS ORG, V28, P11
[5]  
HSING YH, 1985, J BIOL CHEM, V260, P14873
[6]  
Jensen PB, 1997, BIOCHEM PHARMACOL, V54, P755
[7]  
LI YY, 1996, PHARM ADV, V20, P138
[8]  
LIU XM, 1991, CANCER, V10, P220
[9]  
LOCK RB, 1987, ANTI-CANCER DRUG DES, V2, P151
[10]  
NICHOLAS RC, 1980, SCIENCE, V207, P953