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Elife ; 3: e01879, 2014 Jan 01.
Article in English | MEDLINE | ID: mdl-24596153

ABSTRACT

Like other intracellular fusion events, the homotypic fusion of yeast vacuoles requires a Rab GTPase, a large Rab effector complex, SNARE proteins which can form a 4-helical bundle, and the SNARE disassembly chaperones Sec17p and Sec18p. In addition to these proteins, specific vacuole lipids are required for efficient fusion in vivo and with the purified organelle. Reconstitution of vacuole fusion with all purified components reveals that high SNARE levels can mask the requirement for a complex mixture of vacuole lipids. At lower, more physiological SNARE levels, neutral lipids with small headgroups that tend to form non-bilayer structures (phosphatidylethanolamine, diacylglycerol, and ergosterol) are essential. Membranes without these three lipids can dock and complete trans-SNARE pairing but cannot rearrange their lipids for fusion. DOI: http://dx.doi.org/10.7554/eLife.01879.001.


Subject(s)
Membrane Fusion , Membrane Lipids/metabolism , Membranes, Artificial , Q-SNARE Proteins/metabolism , R-SNARE Proteins/metabolism , Vacuoles/metabolism , Adenosine Triphosphatases/metabolism , Binding Sites , Membrane Lipids/chemistry , Molecular Structure , Protein Binding , Protein Conformation , Proteolipids/metabolism , Q-SNARE Proteins/chemistry , R-SNARE Proteins/chemistry , Saccharomyces cerevisiae Proteins/metabolism , Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins/metabolism , Time Factors , Vacuoles/chemistry , Vesicular Transport Proteins/metabolism
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