2I24
Crystal structure analysis of the nurse shark New Antigen Receptor PBLA8 variable domain
Summary for 2I24
Entry DOI | 10.2210/pdb2i24/pdb |
Related | 2I25 2I26 2I27 |
Descriptor | New Antigen Receptor PBLA8, CHLORIDE ION (3 entities in total) |
Functional Keywords | immunoglobulin fold, immune system |
Biological source | Ginglymostoma cirratum (nurse shark) |
Total number of polymer chains | 1 |
Total formula weight | 13473.26 |
Authors | Stanfield, R.L.,Wilson, I.A. (deposition date: 2006-08-15, release date: 2007-03-06, Last modification date: 2024-10-16) |
Primary citation | Stanfield, R.L.,Dooley, H.,Verdino, P.,Flajnik, M.F.,Wilson, I.A. Maturation of Shark Single-domain (IgNAR) Antibodies: Evidence for Induced-fit Binding J.Mol.Biol., 367:358-372, 2007 Cited by PubMed Abstract: Sharks express an unusual heavy-chain isotype called IgNAR, whose variable regions bind antigen as independent soluble domains. To further probe affinity maturation of the IgNAR response, we structurally characterized the germline and somatically matured versions of a type II variable (V) region, both in the presence and absence of its antigen, hen egg-white lysozyme. Despite a disulfide bond linking complementarity determining regions (CDRs) 1 and 3, both germline and somatically matured V regions displayed significant structural changes in these CDRs upon complex formation with antigen. Somatic mutations in the IgNAR V region serve to increase the number of contacts with antigen, as reflected by a tenfold increase in affinity, and one of these mutations appears to stabilize the CDR3 region. In addition, a residue in the HV4 loop plays an important role in antibody-antigen interaction, consistent with the high rate of somatic mutations in this non-CDR loop. PubMed: 17258766DOI: 10.1016/j.jmb.2006.12.045 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.35 Å) |
Structure validation
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