Identification of mammalian mitochondrial proteins that interact with IAPs via N-terminal IAP binding motifs
Details
Publication Year 2007-02,Volume 14,Issue #2,Page 348-357
Journal Title
CELL DEATH AND DIFFERENTIATION
Publication Type
Journal Article
Abstract
Direct IAP binding protein with low pI/second mitochondrial activator of caspases, HtrA2/Omi and GstPT/eRF3 are mammalian proteins that bind via N-terminal inhibitor of apoptosis protein (IAP) binding motifs (IBMs) to the baculoviral IAP repeat (BIR) domains of IAPs. These interactions can prevent IAPs from inhibiting caspases, or displace active caspases, thereby promoting cell death. We have identified several additional potential IAP antagonists, including glutamate dehydrogenase (GdH), Nipsnap 3 and 4, CLPX, leucine-rich pentatricopeptide repeat motif-containing protein and 3-hydroxyisobutyrate dehydrogenase. All are mitochondrial proteins from which N-terminal import sequences are removed generating N-terminal IBMs. Whereas most of these proteins have alanine at the N-terminal position, as observed for previously described antagonists, GdH has an N-terminal serine residue that is essential for X-linked IAP (XIAP) interaction. These newly described IAP binding proteins interact with XIAP mainly via BIR2, with binding eliminated or significantly reduced by a single point mutation (D214S) within this domain. Through this interaction, many are able to antagonise XIAP inhibition of caspase 3 in vitro.
Publisher
NATURE PUBLISHING GROUP
Keywords
ANTI-APOPTOTIC ACTIVITY; SERINE-PROTEASE; CASPASE ACTIVATION; STRUCTURAL BASIS; GRANZYME-B; ML-IAP; INHIBITOR; XIAP; SMAC/DIABLO; REAPER
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Creation Date: 2007-02-01 12:00:00
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