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7JKQ

Human DPP9-CARD8 complex

Summary for 7JKQ
Entry DOI10.2210/pdb7jkq/pdb
EMDB information22367 22974
DescriptorDipeptidyl peptidase 9, Caspase recruitment domain-containing protein 8 (2 entities in total)
Functional Keywordscard8, dpp9, inflammasome, val-boropro (vbp), talabostat, innate immunity, immune system, hydrolase
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains4
Total formula weight318202.39
Authors
Sharif, H.,Hollingsworth, L.R. (deposition date: 2020-07-28, release date: 2021-05-26, Last modification date: 2024-03-06)
Primary citationSharif, H.,Hollingsworth, L.R.,Griswold, A.R.,Hsiao, J.C.,Wang, Q.,Bachovchin, D.A.,Wu, H.
Dipeptidyl peptidase 9 sets a threshold for CARD8 inflammasome formation by sequestering its active C-terminal fragment.
Immunity, 54:1392-, 2021
Cited by
PubMed Abstract: CARD8 detects intracellular danger signals and forms a caspase-1 activating inflammasome. Like the related inflammasome sensor NLRP1, CARD8 autoprocesses into noncovalently associated N-terminal (NT) and C-terminal (CT) fragments and binds the cellular dipeptidyl peptidases DPP8 and 9 (DPP8/9). Certain danger-associated signals, including the DPP8/9 inhibitor Val-boroPro (VbP) and HIV protease, induce proteasome-mediated NT degradation and thereby liberate the inflammasome-forming CT. Here, we report cryoelectron microscopy (cryo-EM) structures of CARD8 bound to DPP9, revealing a repressive ternary complex consisting of DPP9, full-length CARD8, and CARD8-CT. Unlike NLRP1-CT, CARD8-CT does not interact with the DPP8/9 active site and is not directly displaced by VbP. However, larger DPP8/9 active-site probes can directly weaken this complex in vitro, and VbP itself nevertheless appears to disrupt this complex, perhaps indirectly, in cells. Thus, DPP8/9 inhibitors can activate the CARD8 inflammasome by promoting CARD8 NT degradation and by weakening ternary complex stability.
PubMed: 34019797
DOI: 10.1016/j.immuni.2021.04.024
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.3 Å)
Structure validation

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