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-Structure paper
タイトル | Structural basis of soluble membrane attack complex packaging for clearance. |
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ジャーナル・号・ページ | Nat Commun, Vol. 12, Issue 1, Page 6086, Year 2021 |
掲載日 | 2021年10月19日 |
著者 | Anaïs Menny / Marie V Lukassen / Emma C Couves / Vojtech Franc / Albert J R Heck / Doryen Bubeck / |
PubMed 要旨 | Unregulated complement activation causes inflammatory and immunological pathologies with consequences for human disease. To prevent bystander damage during an immune response, extracellular ...Unregulated complement activation causes inflammatory and immunological pathologies with consequences for human disease. To prevent bystander damage during an immune response, extracellular chaperones (clusterin and vitronectin) capture and clear soluble precursors to the membrane attack complex (sMAC). However, how these chaperones block further polymerization of MAC and prevent the complex from binding target membranes remains unclear. Here, we address that question by combining cryo electron microscopy (cryoEM) and cross-linking mass spectrometry (XL-MS) to solve the structure of sMAC. Together our data reveal how clusterin recognizes and inhibits polymerizing complement proteins by binding a negatively charged surface of sMAC. Furthermore, we show that the pore-forming C9 protein is trapped in an intermediate conformation whereby only one of its two transmembrane β-hairpins has unfurled. This structure provides molecular details for immune pore formation and helps explain a complement control mechanism that has potential implications for how cell clearance pathways mediate immune homeostasis. |
リンク | Nat Commun / PubMed:34667172 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.27 - 3.83 Å |
構造データ | EMDB-12646: EMDB-12647: EMDB-12648: EMDB-12649: EMDB-12650, PDB-7nyc: EMDB-12651, PDB-7nyd: |
化合物 | ChemComp-MAN: ChemComp-CA: ChemComp-NAG: ChemComp-FUC: |
由来 |
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キーワード | IMMUNE SYSTEM / Complement / MACPF / Membrane Attack Complex / CDC / pore forming |