A minimal system allowing tubulation with molecular motors pulling on giant liposomes

被引:228
作者
Roux, A
Cappello, G
Cartaud, J
Prost, J
Goud, B
Bassereau, P
机构
[1] Inst Curie, CNRS, UMR 168, Lab PhysicoChim Curie, F-75248 Paris 05, France
[2] Univ Paris 06, CNRS, UMR 7592, Inst Jacques Monod,Lab Biol Cellulaire Mol, F-75251 Paris 05, France
[3] Univ Paris 07, CNRS, UMR 7592, Inst Jacques Monod,Lab Biol Cellulaire Mol, F-75251 Paris 05, France
[4] Inst Curie, CNRS, UMR 144, Lab Mecanismes Mol Transport Intracellulaire, F-75248 Paris 05, France
关键词
D O I
10.1073/pnas.082107299
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The elucidation of physical and molecular mechanisms by which a membrane tube is generated from a membrane reservoir is central to the understanding of the structure and dynamics of intracellular organelles and of transport intermediates in eukaryotic cells. Compelling evidence exists that molecular motors of the dynein and kinesin families are involved in the tubulation of organelles. Here, we show that lipid giant unilamellar vesicles (GUVs), to which kinesin molecules have been attached by means of small polystyrene beads, give rise to membrane tubes and to complex tubular networks when incubated in vitro with microtubules and ATP. Similar tubes and networks are obtained with GUVs made of purified Golgi lipids, as well as with Golgi membranes. No tube formation was observed when kinesins were directly bound to the GUV membrane, suggesting that it is critical to distribute the load on both lipids and motors by means of beads. A kinetic analysis shows that network growth occurs in two phases: a phase in which membrane-bound beads move at the same velocity than free beads, followed by a phase in which the tube growth rate decreases and strongly fluctuates. Our work demonstrates that the action of motors bound to a lipid bilayer is sufficient to generate membrane tubes and opens the way to well controlled experiments aimed at the understanding of basic mechanisms in intracellular transport.
引用
收藏
页码:5394 / 5399
页数:6
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