A convenient large-scale method for the isolation of membrane vesicles permeable to a specific inorganic ion: Isolation and characterization of functional acetylcholine receptor-containing vesicles from the electric organ of Electrophorus electricus

✍ Scribed by Alan B. Sachs; Bernard Lenchitz; Richard L. Noble; George P. Hess

• Publisher: Elsevier Science
• Year: 1982
• Tongue: English
• Weight: 565 KB
• Volume: 124
• Category: Article
• ISSN: 0003-2697
• DOI: 10.1016/0003-2697(82)90236-6

✦ Synopsis

A convenient, large-scale method for the isolation of membrane vesicles permeable to specific inorganic ions has been developed. The general principle of this method involves the exchange of Na+ within the vesicles for external Cs+. Vesicles in which this exchange rapidly occurs can be separated on the basis of their density from vesicles in which the exchange occurs slowly (G. P. Hess and J. P. Andrews (1977) Proc. Nat. Acad. Sci. USA 74,[482][483][484][485][486]. This approach has been adapted to develop a method suitable for the large-scale isolation of vesicles that contain functional acetylcholine receptors from the Electrophorus electricus electroplax. The new procedure involves a discontinuous sucrose gradient for an initial purification of the vesicles. This allows the use of a low-speed centrifuge, which has a capacity up to 30 times greater than the Beckman ultracentrifuge previously used. A self-forming CsCl-Percoll gradient and low-speed centrifugation are then used for the isolation of the functional acetylcholine receptor-containing vesicles. The isolation step leads close to the theoretically possible fourfold purification of the vesicles that contain functional receptors. The yield, up to 12 mg membrane protein/centrifugal run, is about lOO-fold higher than the yield from the sucrose-CsC1 density gradient previously (Hess and Andrews, see above) used. The gradients are self-forming and an equilibrium is reached after centrifugation for only 30 min. In 12 experiments with membrane preparations from 12 different eels, the functional vesicles had an internal volume of 2.0 + 0.3 pl/mg vesicle protein and a receptor concentration of 1.2 + 0.02 pM (1.2 rmol/liter of internal volume). Electron micrographs of these vesicles show an average vesicle radius of 1600 + 300 A. From these results, an average of 12 receptor molecules/membrane vesicle is calculated.