Identification of promiscuous small molecule activators in high-throughput enzyme activation screens

被引:25
作者
Goode, David R. [1 ]
Totten, Ryan K. [1 ]
Heeres, James T. [2 ]
Hergenrothert, Paul J. [1 ,2 ]
机构
[1] Univ Illinois, Roger Adams Lab, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Roger Adams Lab, Dept Biochem, Urbana, IL 61801 USA
关键词
D O I
10.1021/jm701583b
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
It is recognized that high-throughput enzyme inhibition screens often return nonspecific inhibitors as. "hits". Recently, high-throughput screens for enzyme activators have led to the identification of several compounds with novel and potent biological activity. Here, we show that enzyme activation screens can also uncover compounds that activate multiple enzymes in a nonspecific fashion. Described herein are the general structural features of such compounds and methods to differentiate between specific and general enzyme activation.
引用
收藏
页码:2346 / 2349
页数:4
相关论文
共 21 条
[1]   High throughput screening in drug discovery [J].
Carnero A. .
Clinical and Translational Oncology, 2006, 8 (7) :482-490
[2]   On the effect of sodium dodecyl sulfate on the structure of β-galactosidase from Escherichia coli.: A fluorescence study [J].
D'Auria, S ;
Di Cesare, N ;
Gryczynski, I ;
Rossi, M ;
Lakowicz, JR .
JOURNAL OF BIOCHEMISTRY, 2001, 130 (01) :13-18
[3]   SENSITIVE NEW SUBSTRATE FOR CHYMOTRYPSIN [J].
DELMAR, EG ;
LARGMAN, C ;
BRODRICK, JW ;
GEOKAS, MC .
ANALYTICAL BIOCHEMISTRY, 1979, 99 (02) :316-320
[4]   NO-independent stimulators and activators of soluble guanylate cyclase:: discovery and therapeutic potential [J].
Evgenov, Oleg V. ;
Pacher, Pal ;
Schmidt, Peter M. ;
Hasko, Gyoergy ;
Schmidt, Harald H. H. W. ;
Stasch, Johannes-Peter .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (09) :755-768
[5]   A detergent-based assay for the detection of promiscuous inhibitors [J].
Feng, Brian Y. ;
Shoichet, Brian K. .
NATURE PROTOCOLS, 2006, 1 (02) :550-553
[6]   A high-throughput screen for aggregation-based inhibition in a large compound library [J].
Feng, Brian Y. ;
Simeonov, Anton ;
Jadhav, Ajit ;
Babaoglu, Kerim ;
Inglese, James ;
Shoichet, Brian K. ;
Austin, Christopher P. .
JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (10) :2385-2390
[7]   High-throughput assays for promiscuous inhibitors [J].
Feng, BY ;
Shelat, A ;
Doman, TN ;
Guy, RK ;
Shoichet, BK .
NATURE CHEMICAL BIOLOGY, 2005, 1 (03) :146-148
[8]   The dual role of CHAPS in the crystallization of stromelysin-3 catalytic domain [J].
Gall, AL ;
Ruff, M ;
Moras, D .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2003, 59 :603-606
[9]   Allosteric activators of glucokinase: Potential role in diabetes therapy [J].
Grimsby, J ;
Sarabu, R ;
Corbett, WL ;
Haynes, NE ;
Bizzarro, FT ;
Coffey, JW ;
Guertin, KR ;
Hilliard, DW ;
Kester, RF ;
Mahaney, PE ;
Marcus, L ;
Qi, LD ;
Spence, CL ;
Tengi, J ;
Magnuson, MA ;
Chu, CA ;
Dvorozniak, MT ;
Matschinsky, FM ;
Grippo, JF .
SCIENCE, 2003, 301 (5631) :370-373
[10]   Small molecule glucokinase activators as glucose lowering agents: A new paradigm for diabetes therapy [J].
Guertin, Kevin R. ;
Grimsby, Joseph .
CURRENT MEDICINAL CHEMISTRY, 2006, 13 (15) :1839-1843