Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-020-20319-5
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dc.titleStructural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8
dc.contributor.authorGong, Qin
dc.contributor.authorRobinson, Kim
dc.contributor.authorXu, Chenrui
dc.contributor.authorHuynh, Phuong Thao
dc.contributor.authorChong, Kelvin Han Chung
dc.contributor.authorTan, Eddie Yong Jun
dc.contributor.authorZhang, Jiawen
dc.contributor.authorBoo, Zhao Zhi
dc.contributor.authorTeo, Daniel Eng Thiam
dc.contributor.authorLay, Kenneth
dc.contributor.authorZhang, Yaming
dc.contributor.authorLim, John Soon Yew
dc.contributor.authorGoh, Wah Ing
dc.contributor.authorWright, Graham
dc.contributor.authorZhong, Franklin L.
dc.contributor.authorReversade, Bruno
dc.contributor.authorWu, Bin
dc.date.accessioned2022-10-11T07:50:40Z
dc.date.available2022-10-11T07:50:40Z
dc.date.issued2021-01-08
dc.identifier.citationGong, Qin, Robinson, Kim, Xu, Chenrui, Huynh, Phuong Thao, Chong, Kelvin Han Chung, Tan, Eddie Yong Jun, Zhang, Jiawen, Boo, Zhao Zhi, Teo, Daniel Eng Thiam, Lay, Kenneth, Zhang, Yaming, Lim, John Soon Yew, Goh, Wah Ing, Wright, Graham, Zhong, Franklin L., Reversade, Bruno, Wu, Bin (2021-01-08). Structural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8. Nature Communications 12 (1) : 188. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-020-20319-5
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/231978
dc.description.abstractNod-like receptor (NLR) proteins activate pyroptotic cell death and IL-1 driven inflammation by assembling and activating the inflammasome complex. Closely related sensor proteins NLRP1 and CARD8 undergo unique auto-proteolysis-dependent activation and are implicated in auto-inflammatory diseases; however, their mechanisms of activation are not understood. Here we report the structural basis of how the activating domains (FIINDUPA-CARD) of NLRP1 and CARD8 self-oligomerize to assemble distinct inflammasome complexes. Recombinant FIINDUPA-CARD of NLRP1 forms a two-layered filament, with an inner core of oligomerized CARD surrounded by an outer ring of FIINDUPA. Biochemically, self-assembled NLRP1-CARD filaments are sufficient to drive ASC speck formation in cultured human cells—a process that is greatly enhanced by NLRP1-FIINDUPA which forms oligomers in vitro. The cryo-EM structures of NLRP1-CARD and CARD8-CARD filaments, solved here at 3.7 Å, uncover unique structural features that enable NLRP1 and CARD8 to discriminate between ASC and pro-caspase-1. In summary, our findings provide structural insight into the mechanisms of activation for human NLRP1 and CARD8 and reveal how highly specific signaling can be achieved by heterotypic CARD interactions within the inflammasome complexes. © 2021, The Author(s).
dc.publisherNature Research
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.typeArticle
dc.contributor.departmentDEPT OF PAEDIATRICS
dc.description.doi10.1038/s41467-020-20319-5
dc.description.sourcetitleNature Communications
dc.description.volume12
dc.description.issue1
dc.description.page188
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