5GKS
Crystal structure of SLE patient-derived anti-DNA antibody
Summary for 5GKS
Entry DOI | 10.2210/pdb5gks/pdb |
Related | 5GKR |
Descriptor | IgG2, Fab (heavy chain), lambda, Fab (light chain), PHOSPHATE ION, ... (4 entities in total) |
Functional Keywords | antibody, lupus, fab, immune system |
Biological source | Homo sapiens More |
Total number of polymer chains | 4 |
Total formula weight | 92881.00 |
Authors | Arimori, T.,Sakakibara, S.,Kikutani, H.,Takagi, J. (deposition date: 2016-07-05, release date: 2017-07-05, Last modification date: 2023-11-08) |
Primary citation | Sakakibara, S.,Arimori, T.,Yamashita, K.,Jinzai, H.,Motooka, D.,Nakamura, S.,Li, S.,Takeda, K.,Katayama, J.,El Hussien, M.A.,Narazaki, M.,Tanaka, T.,Standley, D.M.,Takagi, J.,Kikutani, H. Clonal evolution and antigen recognition of anti-nuclear antibodies in acute systemic lupus erythematosus Sci Rep, 7:16428-16428, 2017 Cited by PubMed Abstract: The evolutional process of disease-associated autoantibodies in systemic lupus erythematosus (SLE) remains to be established. Here we show intraclonal diversification and affinity maturation of anti-nuclear antibody (ANA)-producing B cells in SLE. We identified a panel of monoclonal ANAs recognizing nuclear antigens, such as double-stranded DNA (dsDNA) and ribonucleoproteins (RNPs) from acute SLE subjects. These ANAs had relatively few, but nonetheless critical mutations. High-throughput immunoglobulin sequencing of blood lymphocytes disclosed the existence of sizable ANA lineages shearing critical mutations intraclonally. We further focused on anti-DNA antibodies, which are capable to bind to both single-stranded (ss) and dsDNA at high affinity. Crystal structure and biochemical analysis confirmed a direct role of the mutations in the acquisition of DNA reactivity and also revealed that these anti-DNA antibodies recognized an unpaired region within DNA duplex. Our study unveils the unique properties of high-affinity anti-DNA antibodies that are generated through antigen-driven affinity maturation in acute phase of SLE. PubMed: 29180749DOI: 10.1038/s41598-017-16681-y PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.05 Å) |
Structure validation
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