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Research Article Free access | 10.1172/JCI115294

Characterization of keratocalmin, a calmodulin-binding protein from human epidermis.

J A Fairley, G A Scott, K D Jensen, L A Goldsmith, and L A Diaz

Department of Dermatology, Medical College of Wisconsin, Milwaukee 53226.

Find articles by Fairley, J. in: JCI | PubMed | Google Scholar

Department of Dermatology, Medical College of Wisconsin, Milwaukee 53226.

Find articles by Scott, G. in: JCI | PubMed | Google Scholar

Department of Dermatology, Medical College of Wisconsin, Milwaukee 53226.

Find articles by Jensen, K. in: JCI | PubMed | Google Scholar

Department of Dermatology, Medical College of Wisconsin, Milwaukee 53226.

Find articles by Goldsmith, L. in: JCI | PubMed | Google Scholar

Department of Dermatology, Medical College of Wisconsin, Milwaukee 53226.

Find articles by Diaz, L. in: JCI | PubMed | Google Scholar

Published July 1, 1991 - More info

Published in Volume 88, Issue 1 on July 1, 1991
J Clin Invest. 1991;88(1):315–322. https://doi.org/10.1172/JCI115294.
© 1991 The American Society for Clinical Investigation
Published July 1, 1991 - Version history
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Abstract

Using affinity-purified calmodulin-binding proteins from human epidermis we have developed a monoclonal IgM antibody, ROC 129.1, to a human desmosomal calcmodulin-binding protein. This antibody reacts with a submembranous 250-kD protein from human keratinocytes and stains human epidermis in a "cell-surface pattern". Permeability studies indicated that the epitope with which this monoclonal reacts is on the inner surface of the cell membrane. Immunoelectronmicroscopy localized the antigen to the desmosome. The epitope is restricted to stratified squamous epithelia and arises between 8-12 wk of fetal development. This desmosomal calmodulin-binding protein, which we have termed keratocalmin, may be involved in the calcium-regulated assembly of desmosomes.

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