@article{4c22be77519040ff857016f342998167,
title = "The Structure of the Necrosome RIPK1-RIPK3 Core, a Human Hetero-Amyloid Signaling Complex",
abstract = "The RIPK1-RIPK3 necrosome is an amyloid signaling complex that initiates TNF-induced necroptosis, serving in human immune defense, cancer, and neurodegenerative diseases. RIPK1 and RIPK3 associate through their RIP homotypic interaction motifs with consensus sequences IQIG (RIPK1) and VQVG (RIPK3). Using solid-state nuclear magnetic resonance, we determined the high-resolution structure of the RIPK1-RIPK3 core. RIPK1 and RIPK3 alternately stack (RIPK1, RIPK3, RIPK1, RIPK3, etc.) to form heterotypic β sheets. Two such β sheets bind together along a compact hydrophobic interface featuring an unusual ladder of alternating Ser (from RIPK1) and Cys (from RIPK3). The crystal structure of a four-residue RIPK3 consensus sequence is consistent with the architecture determined by NMR. The RIPK1-RIPK3 core is the first detailed structure of a hetero-amyloid and provides a potential explanation for the specificity of hetero- over homo-amyloid formation and a structural basis for understanding the mechanisms of signal transduction. Solid-state NMR structures of the human necroptosis RIPK1-RIPK3 complex reveal a hetero-oligomeric amyloid signaling complex.",
keywords = "NMR structure, RHIM, RIPK1, RIPK3, SSNMR, X-ray crystallography, functional amyloid, hetero-amyloid, signaling complex, solid state NMR",
author = "Miguel Mompe{\'a}n and Wenbo Li and Jixi Li and S{\'e}gol{\`e}ne Laage and Siemer, {Ansgar B.} and Gunes Bozkurt and Hao Wu and McDermott, {Ann E.}",
note = "Funding Information: This work was supported by grants from the NIH (R01 AI045937) (to H.W. and A.E.M.), the National Science Foundation (MCB 0749381 and MCB 1412253) (to A.E.M.), the National Key Research and Development Program of China (2016YFA0500600), and National Natural Science Foundation of China (31670878) (to J.L.). M.M. acknowledges the Spanish MINECO (CTQ2017-84825-R). A.E.M. is a member of the New York Structural Biology Center (NYSBC). The NYSBC is a STAR center supported by the New York State Office of Science, Technology and Academic Research. Funding Information: This work was supported by grants from the NIH ( R01 AI045937 ) (to H.W. and A.E.M.), the National Science Foundation ( MCB 0749381 and MCB 1412253 ) (to A.E.M.), the National Key Research and Development Program of China ( 2016YFA0500600 ), and National Natural Science Foundation of China ( 31670878 ) (to J.L.). M.M. acknowledges the Spanish MINECO ( CTQ2017-84825-R ). A.E.M. is a member of the New York Structural Biology Center (NYSBC). The NYSBC is a STAR center supported by the New York State Office of Science, Technology and Academic Research. Publisher Copyright: {\textcopyright} 2018 Elsevier Inc.",
year = "2018",
month = may,
day = "17",
doi = "10.1016/j.cell.2018.03.032",
language = "English (US)",
volume = "173",
pages = "1244--1253.e10",
journal = "Cell",
issn = "0092-8674",
publisher = "Cell Press",
number = "5",
}