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5MU2

ACC1 Fab fragment in complex with CII583-591 (CG10)

Summary for 5MU2
Entry DOI10.2210/pdb5mu2/pdb
DescriptorACC1 Fab fragment heavy chain, ACC1 Fab fragment light chain, synthetic peptide containing the CII583-591 epitope of collagen type II, ... (4 entities in total)
Functional Keywordsanti-citrullinated protein antibody (acpa) fab fragment collagen type ii, immune system
Biological sourceMus musculus (House mouse)
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Total number of polymer chains24
Total formula weight398186.26
Authors
Dobritzsch, D.,Holmdahl, R.,Ge, C. (deposition date: 2017-01-12, release date: 2017-07-19, Last modification date: 2024-01-17)
Primary citationGe, C.,Tong, D.,Liang, B.,Lonnblom, E.,Schneider, N.,Hagert, C.,Viljanen, J.,Ayoglu, B.,Stawikowska, R.,Nilsson, P.,Fields, G.B.,Skogh, T.,Kastbom, A.,Kihlberg, J.,Burkhardt, H.,Dobritzsch, D.,Holmdahl, R.
Anti-citrullinated protein antibodies cause arthritis by cross-reactivity to joint cartilage.
JCI Insight, 2:-, 2017
Cited by
PubMed Abstract: Today, it is known that autoimmune diseases start a long time before clinical symptoms appear. Anti-citrullinated protein antibodies (ACPAs) appear many years before the clinical onset of rheumatoid arthritis (RA). However, it is still unclear if and how ACPAs are arthritogenic. To better understand the molecular basis of pathogenicity of ACPAs, we investigated autoantibodies reactive against the C1 epitope of collagen type II (CII) and its citrullinated variants. We found that these antibodies are commonly occurring in RA. A mAb (ACC1) against citrullinated C1 was found to cross-react with several noncitrullinated epitopes on native CII, causing proteoglycan depletion of cartilage and severe arthritis in mice. Structural studies by X-ray crystallography showed that such recognition is governed by a shared structural motif "RG-TG" within all the epitopes, including electrostatic potential-controlled citrulline specificity. Overall, we have demonstrated a molecular mechanism that explains how ACPAs trigger arthritis.
PubMed: 28679953
DOI: 10.1172/jci.insight.93688
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

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