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Deletion of hinge region of human myeloma lgG1 molecule (protein LEC) associated with nonexpression of G1m(3) and Km(1,2) allotypes. A possible genetic explanation at the DNA level

✍ Scribed by C. Rivat; Liliane Rivat; C. Ropartz; Claudine Schiff; M. Fougereau


Publisher
John Wiley and Sons
Year
1976
Tongue
English
Weight
795 KB
Volume
6
Category
Article
ISSN
0014-2980

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✦ Synopsis


Abstract

In this paper we report the structural basis for the nonexpression of G1m(3) and Km(1, 2) allotypes in an IgG1 (K) human myeloma protein (protein LEC). Heavy and light chains spontaneously dissociate in sodium dodecyl sulfate polyacrylamide gels. Light chains appear to be covalently S‐S bonded. Analysis of cysteine‐containing peptides shows that the heavy chain of the IgG protein LEC has a deletion of residues 21 6‐230, thus encompassing the entire hinge region. An arginine residue, characteristic of the G1m(3) marker is present at position 214. An alanine at position 153 and a leucine at position 191 of the light chain, characteristic of the Km (1, 2) allotypes, are present. It is likely that the double Km and Gm lack of expression is the result of the deletion. The genetic implications of the sequence of this protein are discussed.