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From the Division of Biology, California Institute of Technology, Pasadena, California 91125, and the Institute for Cancer Research, Philadelphia, Pennsylvania 19111
Abstract
The N-terminal sequences from heavy variable regions of 47 myeloma proteins of the NZB mouse have been analyzed. Sixteen of these VH regions have unblocked
amino groups and have been analyzed over their N-terminal 20 residues by automatic sequence analysis. These sequence data along with the antigen-binding profiles and immunoglobulin class distribution are compared with comparable data from BALB/c myeloma proteins. These comparisons suggest that the NZB and BALB/c populations of myeloma proteins are distinct from one another. The genetic implications of this conclusion are discussed.
Footnotes
1 This work was supported by National Institutes of Health Grant AI-10781 and National Science Foundation Grant PCM 76-81542.
2 Present address: Department of Biochemistry, Stanford University School of Medicine, Stanford, California 94305.
3 Present address: Department of Mathematics, California State Polytechnic University, San Luis Obispo, California 93407.
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