Effects of divalent ions on vesicle-vesicle fusion studied by a new luminescence assay for fusion

Abstract

Summary. A new assay has been developed for vesicle-vesicle fusion based upon the mixing of intravesicular contents of two sets of vesicles. Purified firefly luciferase and MgC12 were incorporated into one set of vesicles (LV) and ATP into the other (AV). Vesicles were prepared from soybean phospholipids. The luminescence that resulted from hydrolysis of ATP by luciferase was measured to determine the extent of mixing of the intravesicular contents. In the absence of divalent ions, incubation of a mixture of LV and AV did not produce luminescence. However, if Ca + § or other divalent ions were present at miltimolar concentrations, luminescence occurred. The luminescence did not result from extravesicular reaction of vesicle contents that had leaked into the medium. Instead, luminescence resulted from the mixing of intravesicular spaces of AV and LV in fused vesicles. Optical density changes and negative stain electron microscopy indicated that Ca § + induced extensive aggregation of vesicles. However, quantitation of the maximum possible luminescence indicates that only a small percentage (less than 1%) of the vesicles actually fused in a fusion experiment. Addition of EDTA to chelate Ca ++ after luminescence had been induced resulted in a two- to threefold increase in light emission which then rapidly decayed. These results suggest that the sudden removal of Ca § § caused a transient increase in fusion after which subsequent fusion was inhibited. It was also found that the vesicles were relatively stable to hypotonic solutions.