4.8 Article

The Structure of the Necrosome RIPK1-RIPK3 Core, a Human Hetero-Amyloid Signaling Complex

Journal

CELL
Volume 173, Issue 5, Pages 1244-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2018.03.032

Keywords

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Funding

  1. NIH [R01 AI045937]
  2. National Science Foundation [MCB 0749381, MCB 1412253]
  3. National Key Research and Development Program of China [2016YFA0500600]
  4. National Natural Science Foundation of China [31670878]
  5. Spanish MINECO [CTQ2017-84825-R]
  6. New York State Office of Science, Technology and Academic Research
  7. Direct For Biological Sciences
  8. Div Of Molecular and Cellular Bioscience [1412253] Funding Source: National Science Foundation

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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 beta sheets. Two such beta 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 heteroover homo-amyloid formation and a structural basis for understanding the mechanisms of signal transduction.

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