例如:"lncRNA", "apoptosis", "WRKY"

Traffic of p24 Proteins and COPII Coat Composition Mutually Influence Membrane Scaffolding.

Curr. Biol.2015 May 18;25(10):1296-305. Epub 2015 Apr 30
Jennifer G D'Arcangelo 1 , Jonathan Crissman 1 , Silvere Pagant 1 , Alenka Čopič 1 , Catherine F Latham 1 , Erik L Snapp 2 , Elizabeth A Miller 3
Jennifer G D'Arcangelo 1 , Jonathan Crissman 1 , Silvere Pagant 1 , Alenka Čopič 1 , Catherine F Latham 1 , Erik L Snapp 2 , Elizabeth A Miller 3
+ et al

[No authors listed]

Author information
  • 1 Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
  • 2 Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
  • 3 Department of Biological Sciences, Columbia University, New York, NY 10027, USA. Electronic address: em2282@columbia.edu.

摘要


Eukaryotic protein secretion requires efficient and accurate delivery of diverse secretory and membrane proteins. This process initiates in the ER, where vesicles are sculpted by the essential COPII coat. The Sec13p subunit of the COPII coat contributes to membrane scaffolding, which enforces curvature on the nascent vesicle. A requirement for Sec13p can be bypassed when traffic of lumenally oriented membrane proteins is abrogated. Here we sought to further explore the impact of cargo proteins on vesicle formation. We show that efficient ER export of the p24 family of proteins is a major driver of the requirement for Sec13p. The scaffolding burden presented by the p24 complex is met in part by the cargo adaptor Lst1p, which binds to a subset of cargo, including the p24 proteins. We propose that the scaffolding function of Lst1p is required to generate vesicles that can accommodate difficult cargo proteins that include large oligomeric assemblies and asymmetrically distributed membrane proteins. Vesicles that contain such cargoes are also more dependent on scaffolding by Sec13p, and may serve as a model for large carrier formation in other systems.

基因