Small Molecule Active Site Directed Tools for Studying Human Caspases

被引:65
作者
Poreba, Marcin [1 ]
Szalek, Aleksandra [1 ]
Kasperkiewicz, Paulina [1 ]
Rut, Wioletta [1 ]
Salvesen, Guy S. [2 ]
Drag, Marcin [1 ]
机构
[1] Wroclaw Univ Technol, Dept Bioorgan Chem, Fac Chem, PL-50370 Wroclaw, Poland
[2] Sanford Burnham Prebys Med Discovery Inst, Program Cell Death & Survival Networks, La Jolla, CA 92037 USA
关键词
INTERLEUKIN-1-BETA CONVERTING-ENZYME; RESONANCE-ENERGY-TRANSFER; FLUOROCHROME-LABELED INHIBITORS; ACTIVITY-BASED PROBES; DIPEPTIDYL ASPARTYL FLUOROMETHYLKETONES; GREEN FLUORESCENT PROTEIN; STREPTOMYCES SP E-1511; STRUCTURE-BASED DESIGN; SOLID-PHASE SYNTHESIS; BICYCLIC PEPTIDOMIMETIC COMPOUNDS;
D O I
10.1021/acs.chemrev.5b00434
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Caspases are proteases of clan CD and were described for the first time more than two decades ago. They play critical roles in the control of regulated cell death pathways including apoptosis and inflammation. Due to their involvement in the development of various diseases like cancer, neurodegenerative diseases, or autoimmune disorders, caspases have been intensively investigated as potential drug targets, both in academic and industrial laboratories. This review presents a thorough, deep, and systematic assessment of all technologies developed over the years for the investigation of caspase activity and specificity using substrates and inhibitors, as well as activity based probes, which in recent years have attracted considerable interest due to their usefulness in the investigation of biological functions of this family of enzymes.
引用
收藏
页码:12546 / 12629
页数:84
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