Literature DB >> 7596430

Identification and inhibition of the ICE/CED-3 protease necessary for mammalian apoptosis.

D W Nicholson1, A Ali, N A Thornberry, J P Vaillancourt, C K Ding, M Gallant, Y Gareau, P R Griffin, M Labelle, Y A Lazebnik.   

Abstract

The protease responsible for the cleavage of poly(ADP-ribose) polymerase and necessary for apoptosis has been purified and characterized. This enzyme, named apopain, is composed of two subunits of relative molecular mass (M(r)) 17K and 12K that are derived from a common proenzyme identified as CPP32. This proenzyme is related to interleukin-1 beta-converting enzyme (ICE) and CED-3, the product of a gene required for programmed cell death in Caenorhabditis elegans. A potent peptide aldehyde inhibitor has been developed and shown to prevent apoptotic events in vitro, suggesting that apopain/CPP32 is important for the initiation of apoptotic cell death.

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Year:  1995        PMID: 7596430     DOI: 10.1038/376037a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  873 in total

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5.  Ribozyme-mediated inhibition of caspase-3 protects cerebellar granule cells from apoptosis induced by serum-potassium deprivation.

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8.  Role for caspase-mediated cleavage of Rad51 in induction of apoptosis by DNA damage.

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9.  Mitochondrial regulation of cell death: mitochondria are essential for procaspase 3-p21 complex formation to resist Fas-mediated cell death.

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10.  Presence of a pre-apoptotic complex of pro-caspase-3, Hsp60 and Hsp10 in the mitochondrial fraction of jurkat cells.

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Journal:  EMBO J       Date:  1999-04-15       Impact factor: 11.598

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