Single-molecule FRET study of SNARE-mediated membrane fusion

被引:21
作者
Diao, Jiajie [1 ,2 ]
Ishitsuka, Yuji [1 ,2 ,3 ]
Bae, Woo-Ri [4 ]
机构
[1] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[2] Univ Illinois, Ctr Phys Living Cells, Urbana, IL 61801 USA
[3] Univ Illinois, Howard Hughes Med Inst, Urbana, IL 61801 USA
[4] Korea Adv Inst Sci & Technol, Dept Phys, Taejon 305701, South Korea
基金
美国国家卫生研究院;
关键词
fluorescence resonance energy transfer (FRET); membrane fusion; single molecule; soluble N-ethylmaleimide-sensitive factor-attachment protein receptor (SNARE); ALTERNATING-LASER EXCITATION; RESONANCE ENERGY-TRANSFER; VESICLE FUSION; COMPLEXIN BINDING; FLUORESCENCE; PROTEINS; SYNAPTOTAGMIN; RESOLUTION; REVEALS; DRIVEN;
D O I
10.1042/BSR20110011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane fusion is one of the most important cellular processes by which two initially distinct lipid bilayers merge their hydrophobic cores, resulting in one interconnected structure. Proteins, called SNARE (soluble N-ethylmaleimide-sensitive factor-attachment protein receptor), play a central role in the fusion process that is also regulated by several accessory proteins. In order to study the SNARE-mediated membrane fusion, the in vitro protein reconstitution assay involving ensemble FRET (fluorescence resonance energy transfer) has been used over a decade. In this mini-review, we describe several single-molecule-based FRET approaches that have been applied to this field to overcome the shortage of the bulk assay in terms of protein and fusion dynamics.
引用
收藏
页码:457 / 463
页数:7
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