Literature DB >> 22653732

Membrane fusion intermediates via directional and full assembly of the SNARE complex.

Javier M Hernandez1, Alexander Stein, Elmar Behrmann, Dietmar Riedel, Anna Cypionka, Zohreh Farsi, Peter J Walla, Stefan Raunser, Reinhard Jahn.   

Abstract

Cellular membrane fusion is thought to proceed through intermediates including docking of apposed lipid bilayers, merging of proximal leaflets to form a hemifusion diaphragm, and fusion pore opening. A membrane-bridging four-helix complex of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) mediates fusion. However, how assembly of the SNARE complex generates docking and other fusion intermediates is unknown. Using a cell-free reaction, we identified intermediates visually and then arrested the SNARE fusion machinery when fusion was about to begin. Partial and directional assembly of SNAREs tightly docked bilayers, but efficient fusion and an extended form of hemifusion required assembly beyond the core complex to the membrane-connecting linkers. We propose that straining of lipids at the edges of an extended docking zone initiates fusion.

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Year:  2012        PMID: 22653732      PMCID: PMC3677693          DOI: 10.1126/science.1221976

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  50 in total

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  110 in total

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Review 7.  Energetics, kinetics, and pathway of SNARE folding and assembly revealed by optical tweezers.

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8.  SNARE-mediated membrane fusion arrests at pore expansion to regulate the volume of an organelle.

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Review 9.  The fusion pore, 60 years after the first cartoon.

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10.  Qualitative and quantitative characterization of protein-phosphoinositide interactions with liposome-based methods.

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