A distinct tethering step is vital for vacuole membrane fusion

• Published in: eLife Vol. 3; p. e03251
• Main Authors: Zick, Michael, Wickner, William T
• Format: Journal Article
• Language: English
• Published: England eLife Sciences Publications Ltd 25-09-2014; eLife Sciences Publications, Ltd
• Subjects: assay; Biochemistry; Biomarkers - metabolism; Fluorescent Dyes - metabolism; fusion; Inositol Phosphates - metabolism; Lipids; Lipids - chemistry; membrane; Membrane Fusion; Multiprotein Complexes - metabolism; Protein Binding; Proteins; SNAP receptors; SNARE; Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins - metabolism; tethering; Vacuoles - metabolism; Yeast; fusion; membrane; assay; biochemistry; tethering; S. cerevisiae; SNARE
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/eLife.03251

Past experiments with reconstituted proteoliposomes, employing assays that infer membrane fusion from fluorescent lipid dequenching, have suggested that vacuolar SNAREs alone suffice to catalyze membrane fusion in vitro. While we could replicate these results, we detected very little fusion with the more rigorous assay of lumenal compartment mixing. Exploring the discrepancies between lipid-dequenching and content-mixing assays, we surprisingly found that the disposition of the fluorescent lipids with respect to SNAREs had a striking effect. Without other proteins, the association of SNAREs in trans causes lipid dequenching that cannot be ascribed to fusion or hemifusion. Tethering of the SNARE-bearing proteoliposomes was required for efficient lumenal compartment mixing. While the physiological HOPS tethering complex caused a few-fold increase of trans-SNARE association, the rate of content mixing increased more than 100-fold. Thus tethering has a role in promoting membrane fusion that extends beyond simply increasing the amount of total trans-SNARE complex.