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-Structure paper
タイトル | Structural basis for recognition of N-formyl peptides as pathogen-associated molecular patterns. |
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ジャーナル・号・ページ | Nat Commun, Vol. 13, Issue 1, Page 5232, Year 2022 |
掲載日 | 2022年9月5日 |
著者 | Geng Chen / Xiankun Wang / Qiwen Liao / Yunjun Ge / Haizhan Jiao / Qiang Chen / Yezhou Liu / Wenping Lyu / Lizhe Zhu / Gydo C P van Zundert / Michael J Robertson / Georgios Skiniotis / Yang Du / Hongli Hu / Richard D Ye / |
PubMed 要旨 | The formyl peptide receptor 1 (FPR1) is primarily responsible for detection of short peptides bearing N-formylated methionine (fMet) that are characteristic of protein synthesis in bacteria and ...The formyl peptide receptor 1 (FPR1) is primarily responsible for detection of short peptides bearing N-formylated methionine (fMet) that are characteristic of protein synthesis in bacteria and mitochondria. As a result, FPR1 is critical to phagocyte migration and activation in bacterial infection, tissue injury and inflammation. How FPR1 distinguishes between formyl peptides and non-formyl peptides remains elusive. Here we report cryo-EM structures of human FPR1-Gi protein complex bound to S. aureus-derived peptide fMet-Ile-Phe-Leu (fMIFL) and E. coli-derived peptide fMet-Leu-Phe (fMLF). Both structures of FPR1 adopt an active conformation and exhibit a binding pocket containing the R201XXXR205 (RGIIR) motif for formyl group interaction and receptor activation. This motif works together with D106 for hydrogen bond formation with the N-formyl group and with fMet, a model supported by MD simulation and functional assays of mutant receptors with key residues for recognition substituted by alanine. The cryo-EM model of agonist-bound FPR1 provides a structural basis for recognition of bacteria-derived chemotactic peptides with potential applications in developing FPR1-targeting agents. |
リンク | Nat Commun / PubMed:36064945 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.8 - 2.9 Å |
構造データ | EMDB-31323, PDB-7euo: EMDB-31962, PDB-7vfx: |
化合物 | ChemComp-CLR: ChemComp-PLM: |
由来 |
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キーワード | SIGNALING PROTEIN/IMMUNE SYSTEM / Formyl peptide receptor 1 / Gi complex / SIGNALING PROTEIN / SIGNALING PROTEIN-IMMUNE SYSTEM complex / SIGNALING PROTEIN/PROTEIN BINDING / SIGNALING PROTEIN-PROTEIN BINDING complex |