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8YD7

Structure of FADD/Caspase-8/cFLIP death effector domain assembly

Summary for 8YD7
Entry DOI10.2210/pdb8yd7/pdb
DescriptorCASP8 and FADD-like apoptosis regulator subunit p12, Caspase-8, FAS-associated death domain protein, ... (4 entities in total)
Functional Keywordsfadd, caspase-8, cflip, death effector domain, apoptosis
Biological sourceHomo sapiens (human)
More
Total number of polymer chains10
Total formula weight220627.47
Authors
Lin, S.-C.,Yang, C.-Y. (deposition date: 2024-02-19, release date: 2024-05-15, Last modification date: 2024-10-16)
Primary citationYang, C.Y.,Lien, C.I.,Tseng, Y.C.,Tu, Y.F.,Kulczyk, A.W.,Lu, Y.C.,Wang, Y.T.,Su, T.W.,Hsu, L.C.,Lo, Y.C.,Lin, S.C.
Deciphering DED assembly mechanisms in FADD-procaspase-8-cFLIP complexes regulating apoptosis.
Nat Commun, 15:3791-3791, 2024
Cited by
PubMed Abstract: Fas-associated protein with death domain (FADD), procaspase-8, and cellular FLICE-inhibitory proteins (cFLIP) assemble through death-effector domains (DEDs), directing death receptor signaling towards cell survival or apoptosis. Understanding their three-dimensional regulatory mechanism has been limited by the absence of atomic coordinates for their ternary DED complex. By employing X-ray crystallography and cryogenic electron microscopy (cryo-EM), we present the atomic coordinates of human FADD-procaspase-8-cFLIP complexes, revealing structural insights into these critical interactions. These structures illustrate how FADD and cFLIP orchestrate the assembly of caspase-8-containing complexes and offer mechanistic explanations for their role in promoting or inhibiting apoptotic and necroptotic signaling. A helical procaspase-8-cFLIP hetero-double layer in the complex appears to promote limited caspase-8 activation for cell survival. Our structure-guided mutagenesis supports the role of the triple-FADD complex in caspase-8 activation and in regulating receptor-interacting protein kinase 1 (RIPK1). These results propose a unified mechanism for DED assembly and procaspase-8 activation in the regulation of apoptotic and necroptotic signaling across various cellular pathways involved in development, innate immunity, and disease.
PubMed: 38710704
DOI: 10.1038/s41467-024-47990-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.32 Å)
Structure validation

226707

数据于2024-10-30公开中

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