The history of Z-VAD-FMK, a tool for understanding the significance of caspase inhibition

被引:117
作者
Van Noorden, CJF [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1105 AZ Amsterdam, Netherlands
关键词
proteases; proteinases; caspases-apoptosis; histochemistry; cytochemistry; drug discovery; fluorogenic substrates; chromogenic substrates; protease inhibitors;
D O I
10.1078/0065-1281-00601
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dr. Robert Smith is one of the pioneers in histochemistry. One of his most important achievements is the recognition of proteolysis as a major physiological and pathophysiological process. As a consequence, he developed selective fluorogenic and chromogenic substrates and specific inhibitors of proteases that allow the (histochemical) analysis of protease activity. One of the latest successes is the design of Z-VAD-fluoromethylketone (FMK), the specific caspase inhibitor, that is a key compound for studies on apoptosis. Its development was originally meant for therapeutic use but unforeseen cytotoxicity of a metabolic derivative of the FMK compound disabled its potential as a drug. However, as a tool for fundamental research it is a great success. The history of Z-VAD-FMK is an example of the creative brain and the tireless perseverance of Robert Smith for which histochemistry and cytochemistry owes him so much. This history of Z-VAD-FMK is a well-deserved tribute at the occasion of his 70th birthday.
引用
收藏
页码:241 / 251
页数:11
相关论文
共 41 条
[1]   PEPTIDYL FLUOROMETHYL KETONES AS INHIBITORS OF CATHEPSIN-B - IMPLICATION FOR TREATMENT OF RHEUMATOID-ARTHRITIS [J].
AHMED, NK ;
MARTIN, LA ;
WATTS, LM ;
PALMER, J ;
THORNBURG, L ;
PRIOR, J ;
ESSER, RE .
BIOCHEMICAL PHARMACOLOGY, 1992, 44 (06) :1201-1207
[2]   CELL SUICIDE - BY ICE, NOT FIRE [J].
BARINAGA, M .
SCIENCE, 1994, 263 (5148) :754-756
[3]  
BLACK RA, 1989, J BIOL CHEM, V264, P5323
[4]   ACTIVATION OF INTERLEUKIN-1-BETA BY A CO-INDUCED PROTEASE [J].
BLACK, RA ;
KRONHEIM, SR ;
SLEATH, PR .
FEBS LETTERS, 1989, 247 (02) :386-390
[5]  
BLACK RA, 1988, J BIOL CHEM, V263, P9437
[6]   Different subcellular distribution of caspase-3 and caspase-7 following Fas-induced apoptosis in mouse liver [J].
Chandler, JM ;
Cohen, GM ;
MacFarlane, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (18) :10815-10818
[7]   Caspase inhibitor affords neuroprotection with delayed administration in a rat model of neonatal hypoxic-ischemic brain injury [J].
Cheng, Y ;
Deshmukh, M ;
D'Costa, A ;
Demaro, JA ;
Gidday, JM ;
Shah, A ;
Sun, YL ;
Jacquin, MF ;
Johnson, EM ;
Holtzman, DM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (09) :1992-1999
[8]   T-cell receptor ligation by peptide/MHC induces activation of a caspase in immature thymocytes: The molecular basis of negative selection [J].
Clayton, LK ;
Ghendler, Y ;
Mizoguchi, E ;
Patch, RJ ;
Ocain, TD ;
Orth, K ;
Bhan, AK ;
Dixit, VM ;
Reinherz, EL .
EMBO JOURNAL, 1997, 16 (09) :2282-2293
[9]   Isolation and quantification of fluoroacetate in rat tissues, following dosing of Z-Phe-Ala-CH2-F, a peptidyl fluoromethyl ketone protease inhibitor [J].
Eichhold, TH ;
Hookfin, EB ;
Taiwo, YO ;
De, B ;
Wehmeyer, KR .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1997, 16 (03) :459-467
[10]   CYSTEINE PROTEINASE-INHIBITORS DECREASE ARTICULAR-CARTILAGE AND BONE DESTRUCTION IN CHRONIC INFLAMMATORY ARTHRITIS [J].
ESSER, RE ;
ANGELO, RA ;
MURPHEY, MD ;
WATTS, LM ;
THORNBURG, LP ;
PALMER, JT ;
TALHOUK, JW ;
SMITH, RE .
ARTHRITIS AND RHEUMATISM, 1994, 37 (02) :236-247