Protein-reactive natural products

被引:197
作者
Drahl, C
Cravatt, BF
Sorensen, EJ
机构
[1] Scripps Res Inst, Skaggs Inct Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[4] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
关键词
enzymes; inhibitors; molecular probes; natural products; structure-activity relationships;
D O I
10.1002/anie.200500900
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Researchers in the post-genome era are confronted with the daunting task of assigning structure and function to tens of thousands of encoded proteins. To realize this goal, new technologies are emerging for the analysis of protein function on a global scale, such as activity-based protein profiling (ABPP), which aims to develop active site-directed chemical probes for enzyme analysis in whole proteomes. For the pursuit of such chemical proteomic technologies, it is helpful to derive inspiration from protein-reactive natural products. Natural products use a remarkably diverse set of mechanisms to covalently modify enzymes from distinct mechanistic classes, thus providing a wellspring of chemical concepts that can be exploited for the design of active-site-directed proteomic probes. Herein, we highlight several examples of protein-reactive natural products and illustrate how their mechanisms of action have influenced and continue to shape the progression of chemical proteomic technologies like ABPP. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:5788 / 5809
页数:22
相关论文
共 385 条
[71]   Direct targets of phosphoinositide 3-kinase products in membrane traffic and signal transduction [J].
Corvera, S ;
Czech, MP .
TRENDS IN CELL BIOLOGY, 1998, 8 (11) :442-446
[72]   Regulation and biosynthesis of carbapenem antibiotics in bacteria [J].
Coulthurst, SJ ;
Barnard, AML ;
Salmond, GPC .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (04) :295-306
[73]   Structure and functions of the 20S and 26S proteasomes [J].
Coux, O ;
Tanaka, K ;
Goldberg, AL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :801-847
[74]   IDENTIFICATION AND CHARACTERIZATION OF HYDROPHOBIC MICROCYSTINS IN CANADIAN FRESH-WATER CYANOBACTERIA [J].
CRAIG, M ;
MCCREADY, TL ;
LUU, HA ;
SMILLIE, MA ;
DUBORD, P ;
HOLMES, CFB .
TOXICON, 1993, 31 (12) :1541-1549
[75]   Molecular mechanisms underlying the interaction of motuporin and microycystins with type-1 and type-2A protein phosphatases [J].
Craig, M ;
Luu, HA ;
McCready, TL ;
Williams, D ;
Andersen, RJ ;
Holmes, CFB .
BIOCHEMISTRY AND CELL BIOLOGY, 1996, 74 (04) :569-578
[76]   Lactacystin and clasto-lactacystin beta-lactone modify multiple proteasome beta-subunits and inhibit intracellular protein degradation and major histocompatibility complex class I antigen presentation [J].
Craiu, A ;
Gaczynska, M ;
Akopian, T ;
Gramm, CF ;
Fenteany, G ;
Goldberg, AL ;
Rock, KL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) :13437-13445
[77]   Chemical strategies for the global analysis of protein function [J].
Cravatt, BF ;
Sorensen, EJ .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (06) :663-668
[78]  
DEWITT DL, 1990, J BIOL CHEM, P265
[79]  
Dick LR, 1997, J BIOL CHEM, V272, P182
[80]   Mechanistic studies on the inactivation of the proteasome by lactacystin A central role for clasto-lactacystin beta-lactone [J].
Dick, LR ;
Cruikshank, AA ;
Grenier, L ;
Melandri, FD ;
Nunes, SL ;
Stein, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (13) :7273-7276