Activation of caspases-8 and -10 by FLIP(L).


The first step in caspase activation is transition of the latent zymogen to an active form. For the initiator caspases, this occurs through dimerization of monomeric zymogens at an activating complex. Recent studies have suggested that FLIP(L) [FLICE-like inhibitory protein, long form; FLICE is FADD (Fas-associated death domain protein)-like interleukin-1beta-converting enzyme], previously thought to act solely as an inhibitor of caspase-8 activation, can under certain circumstances function to enhance caspase activation. Using an in vitro induced-proximity assay, we demonstrate that activation of caspases-8 and -10 occurs independently of cleavage of either the caspase or FLIP(L). FLIP(L) activates caspase-8 by forming heterodimeric enzyme molecules with substrate specificity and catalytic activity indistinguishable from those of caspase-8 homodimers. Significantly, the barrier for heterodimer formation is lower than that for homodimer formation, suggesting that FLIP(L) is a more potent activator of caspase-8 than is caspase-8 itself.

6 Figures and Tables

Citations per Year

1,604 Citations

Semantic Scholar estimates that this publication has 1,604 citations based on the available data.

See our FAQ for additional information.

Cite this paper

@article{Boatright2004ActivationOC, title={Activation of caspases-8 and -10 by FLIP(L).}, author={Kelly M Boatright and Cristina E Deis and Jean-Bernard Denault and Daniel P Sutherlin and Guy Salvesen}, journal={The Biochemical journal}, year={2004}, volume={382 Pt 2}, pages={651-7} }