2IMN

Refined crystal structure of a recombinant immunoglobulin domain and a complementarity-determining region 1-grafted mutant

Summary for 2IMN

• Entry DOI: 10.2210/pdb2imn/pdb
• Descriptor: IGA-KAPPA MCPC603 FV (LIGHT CHAIN), SULFATE ION, ACETATE ION, ... (4 entities in total)
• Functional Keywords: immunoglobulin
• Biological source: Mus musculus (house mouse)
• Total number of polymer chains: 1
• Total formula weight: 12460.86

Authors

Steipe, B.,Huber, R. (deposition date: 1992-03-30, release date: 1993-07-15, Last modification date: 2024-06-05)

Primary citation

Steipe, B.,Pluckthun, A.,Huber, R.
Refined crystal structure of a recombinant immunoglobulin domain and a complementarity-determining region 1-grafted mutant.
J.Mol.Biol., 225:739-753, 1992

PubMed Abstract: We report the solution of the crystal structure of a mutant of the immunoglobulin VL domain of the antibody McPC603, in which the complementarity-determining region 1 segment is replaced with that of a different antibody. The wild-type and mutant crystal structures have been refined to a crystallographic R-factor of 14.9% at a nominal resolution of 1.97 A. A detailed description of the structures is given. Crystal packing results in a dimeric association of domains, in a fashion closely resembling that of an Fv fragment. The comparison of this VL domain with the same domain in the Fab fragment of McPC603 shows that the structure of an immunoglobulin VL domain is largely independent of its mode of association, even in places where the inter-subunit contacts are not conserved between VL and VH. In all three complementarity-determining regions we observe conformations that would not have been predicted by the canonical structure hypothesis. Significant differences between the VL domain dimer and the Fab fragment in the third complementarity-determining region show that knowledge of the structure of the dimerization partner and its exact mode of association may be needed to predict the precise conformation of antigen-binding loops.

PubMed: 1602480
DOI: 10.1016/0022-2836(92)90398-4

Experimental method

X-RAY DIFFRACTION (1.97 Å)