Creatine kinase isoenzymes in Torpedo californica: absence of the major brain isoenzyme from nicotinic acetylcholine receptor membranes

• Published in: Biochemistry (Easton) 1986-03, Vol.25 (6), p.1271-1278
• Main Authors: Gysin, Reinhard, Yost, Beverly, Flanagan, Steven D
• Format: Article
• Language: English
• Subjects: acetylcholine; Animals; Antigen-Antibody Complex; Biological and medical sciences; Brain - enzymology; Cell Membrane - metabolism; cell membranes; Cell receptors; Cell structures and functions; creatine kinase; Creatine Kinase - analysis; Cytosol - enzymology; Electric Organ - enzymology; electric organs; Electrophoresis, Polyacrylamide Gel; Fundamental and applied biological sciences. Psychology; Immune Sera; Isoenzymes; Molecular and cellular biology; Molecular Weight; Muscles - enzymology; Organ Specificity; Receptors, Nicotinic - analysis; Torpedo; Torpedo californica
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00354a012

Creatine kinase, actin, and nu 1 are three proteins of Mr 43 000 associated with membranes from electric organ highly enriched in nicotinic acetylcholine receptor. High levels of creatine kinase are required to maintain adequate ATP levels, while actin may play a role in maintaining the synaptic cytoskeleton. Previous investigations have prompted the conclusion that postsynaptic specializations at the receptor-enriched membrane domains in electroplax contain the brain form of creatine kinase rather than the form of creatine kinase predominantly found in muscle. We have examined this conclusion by purifying Torpedo brain creatine kinase to virtual homogeneity in order to examine its immunochemical, molecular, and electrophoretic properties. On the basis of immunological cross-reactivity and isozyme analysis, the receptor-associated creatine kinase is identified to be of the muscle type. When the molecular characteristics of Torpedo brain and muscle creatine kinase are compared, the brain enzyme is positioned at a more basic pH during chromatofocusing and on two-dimensional gel electrophoresis (pI = 7.5-7.9). Furthermore, electrophoretic mobilities of the brain and muscle forms of creatine kinase differ in sodium dodecyl sulfate electrophoresis: the brain isozyme of creatine kinase has lower apparent molecular weight (Mr 41 000) when compared with the muscle enzyme (Mr 43 000). On the basis of the results of our current investigations, the hypothesis that the brain isozyme of creatine kinase is a component of the postsynaptic specializations of the Torpedo californica electroplax must be abandoned. Recent sequence data have established close homology between Torpedo and mammalian muscle creatine kinases. On the basis of electrophoretic criteria, our results indicate that a lower degree of homology exists between the brain isozymes.