SNARE regulators: matchmakers and matchbreakers
pmid: 12914951
SNARE regulators: matchmakers and matchbreakers
SNAREs (soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptors) are membrane-associated proteins that participate in the fusion of internal membranes in eukaryotic cells. SNAREs comprise three distinct and well-conserved families of molecules that act directly as membrane fusogens or, at the least, as elements that bring membranes into close apposition and allow for subsequent fusion events to occur. While the molecular events leading to fusion are still under debate, it is clear that a number of additional factors are required to bring about SNARE-mediated membrane fusion in vivo. Many of these factors, which collectively can be called SNARE regulators (e.g. Sec1/Munc18, synaptotagmin, GATE-16, LMA1, Munc13/UNC-13, synaptophysin, tomosyn, Vsm1, etc.), bind directly to SNAREs and are involved in the regulation of SNARE assembly as well as the ability of SNAREs to participate in trafficking events. In addition, recent studies have suggested a role for posttranslational modification (e.g., phosphorylation) in the regulation of SNARE functions. In this review the possible role of SNARE regulators in SNARE assembly and the involvement of SNARE phosphorylation in the regulation of intracellular membrane trafficking will be discussed.
Synaptophysin, Vesicular Transport Proteins, Munc13, Membrane Proteins, Munc18/Sec1, Biological Transport, Complexin, Cell Biology, Membrane Fusion, Synaptotagmin, LMA1, SNARE, Arf-GAP, Animals, Humans, Tomosyn, Phosphorylation, SNARE Proteins, Apg8/GATE-16, Molecular Biology, Vsm1/Ddi1, Signal Transduction
Synaptophysin, Vesicular Transport Proteins, Munc13, Membrane Proteins, Munc18/Sec1, Biological Transport, Complexin, Cell Biology, Membrane Fusion, Synaptotagmin, LMA1, SNARE, Arf-GAP, Animals, Humans, Tomosyn, Phosphorylation, SNARE Proteins, Apg8/GATE-16, Molecular Biology, Vsm1/Ddi1, Signal Transduction
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