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First published online March 4, 2009


Journal of Cell Science 122, 604e (2009)
© The Company of Biologists Limited
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In this issue

A role for rafts in flagella


Figure 1

The parasite Trypanosoma brucei has a single polarised flagellum that drives cellular motility. Some plasma-membrane-associated proteins localise specifically to the flagellum, but what are the mechanisms responsible for their targeting and retention? On page 859, David Engman and colleagues propose a role for lipid rafts – which are detergent-resistant, highly ordered plasma-membrane microdomains – in targeting flagellar proteins. The authors first show that several molecules that are thought to be raft components are enriched in the flagellum. In addition, they use laurdan (an amphiphilic fluor) to show that the flagellar membrane possesses increased liquid order; together, these data indicate that flagella are enriched in lipid rafts. The authors next show that the flagellar calcium-sensing protein calflagin Tb24 concentrates in detergent-resistant membranes; in an accompanying paper (p. 867), the group shows that calflagin Tb24 must be palmitoylated to localise to flagella, and identifies the specific palmitoyl acyltransferase that modifies it. Importantly, calflagin Tb24 redistributes to other domains when lipid rafts are destabilised. Thus, association with lipid rafts directs the flagellar localisation of calflagin Tb24 and might, the authors propose, be a general mechanism for the trafficking of specific proteins to the membrane of flagella and cilia.


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Related articles in JCS:

Flagellar membrane localization via association with lipid rafts
Kevin M. Tyler, Alina Fridberg, Krista M. Toriello, Cheryl L. Olson, John A. Cieslak, Theodore L. Hazlett, and David M. Engman
JCS 2009 122: 859-866. [Abstract] [Full Text]  

Identification of a palmitoyl acyltransferase required for protein sorting to the flagellar membrane
Brian T. Emmer, Christina Souther, Krista M. Toriello, Cheryl L. Olson, Conrad L. Epting, and David M. Engman
JCS 2009 122: 867-874. [Abstract] [Full Text]  




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