The Structure of the Necrosome RIPK1-RIPK3 core, a human hetero-amyloid signaling complex
| Autor: | Hao Wu, Ségolène Laage, Miguel Mompeán, Ansgar B. Siemer, Jixi Li, Ann E. McDermott, Gunes Bozkurt, Wenbo Li |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Amyloid Necroptosis Amyloidogenic Proteins Apoptosis Crystal structure Biology Crystallography X-Ray General Biochemistry Genetics and Molecular Biology Protein Structure Secondary Article 03 medical and health sciences RIPK1 Necrosis 0302 clinical medicine Consensus sequence Humans Protein Interaction Domains and Motifs Amino Acid Sequence Nuclear Magnetic Resonance Biomolecular Tumor Necrosis Factor-alpha 030104 developmental biology Solid-state nuclear magnetic resonance Receptor-Interacting Protein Serine-Threonine Kinases Core (graph theory) Biophysics Signal transduction Sequence Alignment 030217 neurology & neurosurgery Signal Transduction |
| Popis: | 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 to 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 SSNMR. 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. |
| Databáze: | OpenAIRE |
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