Single secretory granules of live cells recruit syntaxin-1 and synaptosomal associated protein 25 (SNAP-25) in large copy numbers

被引:89
作者
Knowles, M. K. [2 ]
Barg, S. [3 ]
Wan, L. [1 ]
Midorikawa, M. [1 ]
Chen, X. [1 ]
Almers, Wolfhard [1 ]
机构
[1] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97239 USA
[2] Univ Denver, Dept Chem & Biochem, Denver, CO 80208 USA
[3] Uppsala Univ, Dept Med Cell Biol, S-75123 Uppsala, Sweden
基金
美国国家卫生研究院; 日本学术振兴会;
关键词
location-guided averaging; nanodomains; total internal reflection fluorescence; single molecules; single particle tracking; 3 SNARE COMPLEXES; MEMBRANE-FUSION; MOLECULES; EXOCYTOSIS; DYNAMICS; MICROSCOPY; TRACKING; ANATOMY;
D O I
10.1073/pnas.1014840107
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
Before secretory vesicles undergo exocytosis, they must recruit the proteins syntaxin-1 and synaptosomal associated protein 25 (SNAP-25) in the plasma membrane. GFP-labeled versions of both proteins cluster at sites where secretory granules have docked. Single-particle tracking shows that minority populations of both molecules are strongly hindered in their mobility, consistent with their confinement in nanodomains. We measured the fluorescence of granule-associated clusters, the fluorescence of single molecules, and the numbers of unlabeled syntaxin-1 and SNAP-25 molecules per cell. There was a more than 10-fold excess of SNAP-25 over syntaxin-1. Fifty to seventy copies each of syntaxin-1 and SNAP-25 molecules were associated with a single docked granule, many more than have been reported to be required for fusion.
引用
收藏
页码:20810 / 20815
页数:6
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