Structures of proteinase 3 and the CD177 receptor complex reveal a major autoantibody epitope

Read full text
Authors: Céline Zheng, Jana Joha, Maria Carrasquero, Kamel El Omari, E.D. Lowe, Shirish Dubey, Simon J. Draper, Yu-Chi Chang, Hsi-Hsien Lin, AD Salama, Kirsty McHugh, Elena Seiradake
Cited by: 1
References: 112

Abstract

Granulomatosis with polyangiitis is a life-threatening systemic vasculitis, characterised by anti-neutrophil cytoplasmic autoantibodies (ANCA) most commonly against proteinase 3 (PR3), a protease expressed intracellularly and on the surface of neutrophils. Most cell surface PR3 is bound to the receptor CD177; however, the molecular mechanism of the interactions is not well understood. Here, we present crystal structures of CD177 in complex with PR3 and unliganded CD177. We describe a mainly hydrophobic binding interface between PR3 and CD177, involving the first two Ly6/uPAR (LU) domains of CD177. These form a globular structure which is connected to downstream domains via a flexible linker. Using a panel of PR3-ANCA-positive patient samples, we show that a significant proportion of ANCAs target the CD177-binding site of PR3 in these samples. Structure-guided mutation of the CD177-binding site on PR3 is effective in reducing PR3-ANCA binding. The results demonstrate that the CD177-binding surface of PR3 harbours a major PR3-ANCA epitope, and that the extent of binding to this surface varies between different patients.

Fields of Study & Subjects

Vasculitis and related conditions Neutrophil Myeloperoxidase and Oxidative Mechanisms Protease and Inhibitor Mechanisms

Publication details

Journal / source
EMBO Reports
Publisher
Springer Science and Business Media LLC
Volume
27
Issue
6
Pages
1580–1606
Publication date
17 February 2026
Language
EN