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1DL7

THE STRUCTURAL BASIS OF REPERTOIRE SHIFT IN AN IMMUNE RESPONSE TO PHOSPHOCHOLINE

Summary for 1DL7
Entry DOI10.2210/pdb1dl7/pdb
DescriptorPROTEIN (ANTIBODY M3C65 (LIGHT CHAIN)), PROTEIN (ANTIBODY M3C65 (HEAVY CHAIN)), P-NITROPHENYL-PHOSPHOCHOLINE, ... (4 entities in total)
Functional Keywordssingle chain fv, repertoire shift, immune system
Biological sourceMus musculus (mouse)
More
Total number of polymer chains2
Total formula weight24183.92
Authors
Schumacher, M.,Brown, M. (deposition date: 1999-12-08, release date: 2000-12-13, Last modification date: 2024-11-13)
Primary citationBrown, M.,Schumacher, M.A.,Wiens, G.D.,Brennan, R.G.,Rittenberg, M.B.
The structural basis of repertoire shift in an immune response to phosphocholine.
J.Exp.Med., 191:2101-2112, 2000
Cited by
PubMed Abstract: The immune response to phosphocholine (PC)-protein is characterized by a shift in antibody repertoire as the response progresses. This change in expressed gene combinations is accompanied by a shift in fine specificity toward the carrier, resulting in high affinity to PC-protein. The somatically mutated memory hybridoma, M3C65, possesses high affinity for PC-protein and the phenyl-hapten analogue, p-nitrophenyl phosphocholine (NPPC). Affinity measurements using related PC-phenyl analogues, including peptides of varying lengths, demonstrate that carrier determinants contribute to binding affinity and that somatic mutations alter this recognition. The crystal structure of an M3C65-NPPC complex at 2.35-A resolution allows evaluation of the three light chain mutations that confer high-affinity binding to NPPC. Only one of the mutations involves a contact residue, whereas the other two have indirect effects on the shape of the combining site. Comparison of the M3C65 structure to that of T15, an antibody dominating the primary response, provides clear structural evidence for the role of carrier determinants in promoting repertoire shift. These two antibodies express unrelated variable region heavy and light chain genes and represent a classic example of the effect of repertoire shift on maturation of the immune response.
PubMed: 10859335
DOI: 10.1084/jem.191.12.2101
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.35 Å)
Structure validation

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数据于2025-11-05公开中

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