| Literature DB >> 18314058 |
Scott H Kaufmann1, Sun-Hee Lee, X Wei Meng, David A Loegering, Timothy J Kottke, Alexander J Henzing, Sandrine Ruchaud, Kumiko Samejima, William C Earnshaw.
Abstract
Caspases are aspartate-directed cysteine proteases that cleave a diverse group of intracellular substrates to contribute to various manifestations of apoptosis. These proteases are synthesized as inactive precursors and are activated as a consequence of signaling induced by a wide range of physiological and pathological stimuli. Caspase activation can be detected by measurement of catalytic activity, immunoblotting for cleavage of their substrates, immunolabeling using conformation-sensitive antibodies or affinity labeling followed by flow cytometry or ligand blotting. Here we describe methods for each of these assays, identify recent improvements in these assays and outline the strengths and limitations of each approach.Mesh:
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Year: 2008 PMID: 18314058 DOI: 10.1016/j.ymeth.2007.11.005
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608