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      The role of CAP3 in CD95 signaling: new insights into the mechanism of procaspase-8 activation.

      Cell Death and Differentiation
      Amino Acid Chloromethyl Ketones, pharmacology, Antigens, CD95, metabolism, Apoptosis, Caspase 8, Caspase Inhibitors, Caspases, chemistry, Cell Line, Cysteine Proteinase Inhibitors, Death Domain Receptor Signaling Adaptor Proteins, Enzyme Activation, Enzyme Precursors, Humans, Kinetics, Models, Biological, Protein Structure, Tertiary, Serpins, analysis, physiology, Signal Transduction, Tumor Necrosis Factor Receptor-Associated Peptides and Proteins

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          Abstract

          Formation of the CD95 (APO-1/Fas) death inducing signaling complex (DISC) plays a central role in CD95 signaling. Previously, CD95 DISC composition was analyzed by two-dimensional gel electrophoresis and four major cytotoxicity-associated proteins (CAP1-4) were found. CAP1 and CAP2 were defined to be unmodified and phosphorylated FADD, respectively. CAP4 was identified as procaspase-8a. CAP3, however, has remained elusive. In this study, we demonstrate that CAP3 is an intermediate of procaspase-8 processing. CAP3 is generated within seconds of DISC formation and subsequently processed to the prodomain of procaspase-8a that is known as p26 (CAP5). These findings lead to new insights into the mechanism of procaspase-8 processing and apoptosis initiation.

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