JCB logo
Accuri Cytometers
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online 10 July 2000. doi:10.1083/jcb.150.1.105
This Article
Right arrow Full Text
Right arrow Full Text (PDF, 373K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McNew, J. A.
Right arrow Articles by Rothman, J. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McNew, J. A.
Right arrow Articles by Rothman, J. E.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

© The Rockefeller University Press, 0021-9525/2000//105 $5.00
The Journal of Cell Biology, Volume 150, Number 1, , 2000 105-118


Original Article

Close Is Not Enough

: Snare-Dependent Membrane Fusion Requires an Active Mechanism That Transduces Force to Membrane Anchors



James A. McNewa, Thomas Webera, Francesco Parlatia, Robert J. Johnstona, Thomas J. Meliaa, Thomas H. Söllnera, and James E. Rothmana

a Cellular Biochemistry and Biophysics Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021

Is membrane fusion an essentially passive or an active process? It could be that fusion proteins simply need to pin two bilayers together long enough, and the bilayers could do the rest spontaneously. Or, it could be that the fusion proteins play an active role after pinning two bilayers, exerting force in the bilayer in one or another way to direct the fusion process. To distinguish these alternatives, we replaced one or both of the peptidic membrane anchors of exocytic vesicle (v)- and target membrane (t)-SNAREs (soluble N-ethylmaleimide-sensitive fusion protein [NSF] attachment protein [SNAP] receptor) with covalently attached lipids. Replacing either anchor with a phospholipid prevented fusion of liposomes by the isolated SNAREs, but still allowed assembly of trans-SNARE complexes docking vesicles. This result implies an active mechanism; if fusion occurred passively, simply holding the bilayers together long enough would have been sufficient. Studies using polyisoprenoid anchors ranging from 15–55 carbons and multiple phospholipid-containing anchors reveal distinct requirements for anchors of v- and t-SNAREs to function: v-SNAREs require anchors capable of spanning both leaflets, whereas t-SNAREs do not, so long as the anchor is sufficiently hydrophobic. These data, together with previous results showing fusion is inhibited as the length of the linker connecting the helical bundle-containing rod of the SNARE complex to the anchors is increased (McNew, J.A., T. Weber, D.M. Engelman, T.H. Sollner, and J.E. Rothman, 1999. Mol. Cell. 4:415–421), suggests a model in which one activity of the SNARE complex promoting fusion is to exert force on the anchors by pulling on the linkers. This motion would lead to the simultaneous inward movement of lipids from both bilayers, and in the case of the v-SNARE, from both leaflets.

Key Words: lipid mixing • isoprene • liposome • lipid anchor • vesicular transport



© 2000 The Rockefeller University Press

Abbreviations used in this paper: C45, maleimidopropionic acid solanesylester; C55, maleimidopropionic acid undecaprenylester; GPI, glycerophosphoinositide; NBD, nitro-2,1,3-benzoxadiazole; NSF, N-ethylmaleimide sensitive fusion protein; maleimide-PE, maleimide phosphatidylethanolamine derivative; rhodamine, lissamine rhodamine B; SN25 C-S, mutant version of SNAP-25 without any cysteines; SNAP, soluble NSF attachment protein; SNAP-25, synaptosomal-associated proteins of 25 kD; SNARE, SNAP receptor; TMD, transmembrane domain; t-SNARE, target membrane SNARE; v-SNARE, vesicle SNARE; VAMP, vesicle-associated membrane protein.



Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:



  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents