Calcineurin: a member of a family of calmodulin-stimulated protein phosphatases

• Published in: Proceedings of the Society for Experimental Biology and Medicine Vol. 177; no. 1; p. 12
• Main Authors: Manalan, A S, Krinks, M H, Klee, C B
• Format: Journal Article
• Language: English
• Published: United States 01-10-1984
• Subjects: Animals; Brain - enzymology; Calcium - metabolism; Calmodulin-Binding Proteins; Cattle; Cross Reactions; Electrophoresis, Polyacrylamide Gel; Macromolecular Substances; Molecular Weight; Muscles - enzymology; Myocardium - enzymology; Phosphoprotein Phosphatases - analysis
• ISSN: 0037-9727
• DOI: 10.3181/00379727-177-41905

Calcineurin, a major calmodulin-binding protein of brain, is a heterodimer composed of a 61,000 Mr calmodulin-binding subunit, calcineurin A, and a 19,000 Mr Ca2+-binding subunit, calcineurin B. The discovery of a calmodulin-regulated protein phosphatase in rabbit skeletal muscle with a similar subunit structure led to the identification of calcineurin as a protein phosphatase (AA Stewart, TS Ingebritsen, A Manalan, CB Klee, P Cohen (1982) FEBS Lett 137:80-84). Using rabbit polyclonal antibodies to bovine brain calcineurin, both subunits of calcineurin can be identified in crude homogenates of bovine brain by an immunoblotting technique. In crude homogenates of bovine skeletal and cardiac muscle, a 59,000-61,000 Mr doublet and a 15,000 Mr species (the electrophoretic mobility of calcineurin B) are also detected by this technique. The cross-reactivity of these species with antibodies to brain calcineurin indicates antigenic similarity between the muscle proteins and calcineurin, and suggests the existence of a family of structurally related calmodulin-stimulated protein phosphatases. Like calcineurin, the 61,000 Mr subunits in skeletal and cardiac muscle bind calmodulin and are detected in crude tissue extracts by 125I-calmodulin gel overlay. Thus, both the 125I-calmodulin gel overlay method and the immunoblotting technique are useful in screening crude preparations, in which detection of calmodulin-stimulated protein phosphatase activity may be complicated by the many phosphatases present.