Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion

被引:24
|
作者
Lee, Dong Woog [1 ]
Kristiansen, Kai [1 ]
Donaldson, Stephen H., Jr. [1 ]
Cadirov, Nicholas [1 ]
Banquy, Xavier [2 ]
Israelachvili, Jacob N. [3 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Montreal, Fac Pharm, Canada Res Chair Bio Inspired Mat & Interfaces, Montreal, PQ H3C 3J7, Canada
[3] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
MEMBRANE-FUSION; SNARE PROTEINS; LINE TENSION; PC12; CELLS; RAFTS; BILAYERS; ADHESION; CHOLESTEROL; MECHANISMS; EXOCYTOSIS;
D O I
10.1038/ncomms8238
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
Membrane fusion is the core process in membrane trafficking and is essential for cellular transport of proteins and other biomacromolecules. During protein-mediated membrane fusion, membrane proteins are often excluded from the membrane-membrane contact, indicating that local structural transformations in lipid domains play a major role. However, the rearrangements of lipid domains during fusion have not been thoroughly examined. Here using a newly developed Fluorescence Surface Forces Apparatus (FL-SFA), migration of liquid-disordered clusters and depletion of liquid-ordered domains at the membrane-membrane contact are imaged in real time during hemifusion of model lipid membranes, together with simultaneous force-distance and lipid membrane thickness measurements. The load and contact time-dependent hemifusion results show that the domain rearrangements decrease the energy barrier to fusion, illustrating the significance of dynamic domain transformations in membrane fusion processes. Importantly, the FL-SFA can unambiguously correlate interaction forces and in situ imaging in many dynamic interfacial systems.
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页数:8
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