| Literature DB >> 18603133 |
Cristina Pop1, Guy S Salvesen, Fiona L Scott.
Abstract
The measurement of general caspase activity and the quantification of purified recombinant caspases in vitro can be accomplished with relative ease. But the determination of which caspases are active in a cellular context is much more challenging. This is because commercially available small molecule substrates and inhibitors do not display sufficient specificity to dissect the complex interplay of caspase pathways. Here we describe procedures that can be used to validate which caspases are active in cell culture models and determine which caspases are responsible for specific cleavage events. We also recommend methods for working with recombinant initiator caspases in vitro and suggest ways to accurately assess the cleavage efficiency of natural caspase substrates.Mesh:
Substances:
Year: 2008 PMID: 18603133 DOI: 10.1016/S0076-6879(08)01621-2
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600