Transverse tubules from frog skeletal muscle. Purification and properties of vesicles sealed with the inside-out orientation

Abstract

Transverse tubule vesicles were isolated from frog skeletal muscle by a procedure initially described by Rosemblatt (J. Biol. Chem. 256, 8140–8148 (1981)) and later modified by Hidalgo (J. Biol. Chem. 258, 13937–13945 (1983)). A large fraction of the isolated vesicles (80–90%) were sealed, as indicated by the detergent induced increase in (Na+ + K+)-ATPase activity and ATP-dependent ouabain binding. To determine the orientation of the sealed vesicles binding of digoxin, a lipid soluble derivative of ouabain, was measured. The same values of ATP-dependent digoxin binding were found with or without detergents, indicating that all the vesicles that are sealed have the ATP site accessible, and hence are sealed with the cytoplasmic side-out (inside-out orientation). The transverse tubule preparation isolated from frog muscle is highly purified, as indicated by its cholesterol content and its (Na+ + K+)-ATPase activity; negligible contamination with sarcoplasmic reticulum was observed, as indicated by the protein composition and the lack of measurable Ca2+-ATPase activity of the isolated transverse tubules. High initial rates of Mg2+-ATPase activity were found, with the peculiar property of being inhibited during the course of the reaction. Addition of lysophosphatidylcholine or saponin partially prevented the inhibition of Mg2+-ATPase activity during the reaction.