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5MU0

ACC1 Fab fragment in complex with citrullinated C1 epitope of CII (IA03)

Summary for 5MU0
Entry DOI10.2210/pdb5mu0/pdb
Descriptorheavy chain of ACC1 antibody Fab fragment, light chain of ACC1 antibody Fab fragment, IA03 peptide containing the citrullinated C1 epitope of collagen type II,Collagen alpha-1(II) chain,IA03 peptide containing the citrullinated C1 epitope of collagen type II, ... (4 entities in total)
Functional Keywordsanti-citrullinated protein antibody (acpa) fab fragment collagen type ii citrullinated c1 epitope, immune system
Biological sourceMus musculus (House mouse)
More
Total number of polymer chains24
Total formula weight390033.06
Authors
Dobritzsch, D.,Holmdahl, R.,Ge, C. (deposition date: 2017-01-11, 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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