JCB logo
Quantitative Colocalization Analysis Software
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online
doi:10.1083/jcb.1776rr3
The Journal of Cell Biology, Vol. 177, No. 6, 947-
The Rockefeller University Press, 0021-9525 $30.00
© Williams
This Article
Right arrow Full Text (PDF, 1144K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Williams, R.
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?

Research Roundup

Curves are attractive



Figure 1
Membrane-bending proteins (pink) quickly aggregate and vesiculate a membrane (blue/yellow) in silico.

DESERNO/MACMILLAN

Membrane-bending proteins can attract each other when the curves they create overlap, according to a computer simulation by Benedict Reynwar, Markus Deserno, and colleagues (Max Planck Institute, Mainz, Germany).

The energy required for membrane reshaping—as needed for endocytosis, vesiculation, etc.—is too great for one membrane-bending protein alone to achieve, so cooperation is essential. How cooperation occurs, however, has been a bit of a mystery.

Part of the mystery stems from previous theoretical calculations that predicted that curves induced by a membrane-bending protein repel other proteins of its kind. Experimental systems, on the other hand, suggested that membrane curving might be enough to aggregate the responsible proteins. Ruling out other specific protein–protein interactions is difficult, however.

Now, in silico simulations by Reynwar et al. show that, as suggested by experimentation, curves can be enough to pull together membrane benders. The team created computerized proteins that induced a membrane curve geometry similar to that of a real membrane-bending protein called BAR domain. In a simulated lipid bilayer in which the proteins freely diffused, the induced deformed regions encircling the proteins soon overlapped. The proteins did not then diffuse away but instead aggregated such that the area of deformation grew, eventually leading to vesiculation.

The ease with which the simulated proteins aggregated and promoted vesiculation—within just milliseconds—suggests that real cells must keep a tight leash on their benders. Formula

Reference:

Reynwar, B.J., et al. 2007. Nature. 447:461–464.[CrossRef][Medline]



Ruth Williams

ruth.williams{at}rockefeller.edu


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
Right arrow Full Text (PDF, 1144K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Williams, R.
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?


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