Journal article
Reconstituted NALP1 Inflammasome Reveals Two-Step Mechanism of Caspase-1 Activation
B Faustin, L Lartigue, JM Bruey, F Luciano, E Sergienko, B Bailly-Maitre, N Volkmann, D Hanein, I Rouiller, JC Reed
Molecular Cell | CELL PRESS | Published : 2007
Abstract
Interleukin (IL)-1β maturation is accomplished by caspase-1-mediated proteolysis, an essential element of innate immunity. NLRs constitute a recently recognized family of caspase-1-activating proteins, which contain a nucleotide-binding oligomerization domain and leucine-rich repeat (LRR) domains and which assemble into multiprotein complexes to create caspase-1-activating platforms called "inflammasomes." Using purified recombinant proteins, we have reconstituted the NALP1 inflammasome and have characterized the requirements for inflammasome assembly and caspase-1 activation. Oligomerization of NALP1 and activation of caspase-1 occur via a two-step mechanism, requiring microbial product, mu..
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Awarded by National Institutes of Health