8ENU

Structure of the C3bB proconvertase in complex with lufaxin

8ENU の概要

• エントリーDOI: 10.2210/pdb8enu/pdb
• EMDBエントリー: 28279
• 分子名称: Complement C3 beta chain, Complement C3b alpha' chain, Complement factor B, ... (7 entities in total)
• 機能のキーワード: complement, alternative pathway, inhibitor, sand fly, immune system
• 由来する生物種: Lutzomyia longipalpis; 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 296148.26

構造登録者

Andersen, J.F.,Lei, H. (登録日: 2022-09-30, 公開日: 2023-08-09, 最終更新日: 2024-10-23)

主引用文献

Andersen, J.F.,Lei, H.,Strayer, E.C.,Kanai, T.,Pham, V.,Pan, X.Z.,Alvarenga, P.H.,Gerber, G.F.,Asojo, O.A.,Francischetti, I.M.B.,Brodsky, R.A.,Valenzuela, J.G.,Ribeiro, J.M.C.
A bispecific inhibitor of complement and coagulation blocks activation in complementopathy models via a novel mechanism.
Blood, 141:3109-3121, 2023

PubMed Abstract: Inhibitors of complement and coagulation are present in the saliva of a variety of blood-feeding arthropods that transmit parasitic and viral pathogens. Here, we describe the structure and mechanism of action of the sand fly salivary protein lufaxin, which inhibits the formation of the central alternative C3 convertase (C3bBb) and inhibits coagulation factor Xa (fXa). Surface plasmon resonance experiments show that lufaxin stabilizes the binding of serine protease factor B (FB) to C3b but does not detectably bind either C3b or FB alone. The crystal structure of the inhibitor reveals a novel all β-sheet fold containing 2 domains. A structure of the lufaxin-C3bB complex obtained via cryo-electron microscopy (EM) shows that lufaxin binds via its N-terminal domain at an interface containing elements of both C3b and FB. By occupying this spot, the inhibitor locks FB into a closed conformation in which proteolytic activation of FB by FD cannot occur. C3bB-bound lufaxin binds fXa at a separate site in its C-terminal domain. In the cryo-EM structure of a C3bB-lufaxin-fXa complex, the inhibitor binds to both targets simultaneously, and lufaxin inhibits fXa through substrate-like binding of a C-terminal peptide at the active site as well as other interactions in this region. Lufaxin inhibits complement activation in ex vivo models of atypical hemolytic uremic syndrome (aHUS) and paroxysmal nocturnal hemoglobinuria (PNH) as well as thrombin generation in plasma, providing a rationale for the development of a bispecific inhibitor to treat complement-related diseases in which thrombosis is a prominent manifestation.

PubMed: 36947859
DOI: 10.1182/blood.2022019359

実験手法

ELECTRON MICROSCOPY (3.22 Å)