Cell-Derived Vesicles for Single-Molecule Imaging of Membrane Proteins

被引:19
|
作者
Moonschi, Faruk H. [1 ]
Effinger, Amy K. [1 ]
Zhang, Xiaolu [1 ]
Martin, William E. [1 ]
Fox, Ashley M. [1 ]
Heidary, David K. [1 ]
DeRouchey, Jason E. [1 ]
Richards, Christopher I. [1 ]
机构
[1] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
关键词
fluorescence correlation spectroscopy; fluorescence microscopy; transmembrane proteins; single-molecule studies; vesicles; SUBUNIT STOICHIOMETRY; RECEPTOR; MUSCLE;
D O I
10.1002/anie.201408707
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new approach is presented for the application of single-molecule imaging to membrane receptors through the use of vesicles derived from cells expressing fluorescently labeled receptors. During the isolation of vesicles, receptors remain embedded in the membrane of the resultant vesicles, thus allowing these vesicles to serve as nanocontainers for single-molecule measurements. Cell-derived vesicles maintain the structural integrity of transmembrane receptors by keeping them in their physiological membrane. It was demonstrated that receptors isolated in these vesicles can be studied with solution-based fluorescence correlation spectroscopy (FCS) and can be isolated on a solid substrate for single-molecule studies. This technique was applied to determine the stoichiometry of 34 nicotinic receptors. The method provides the capability to extend single-molecule studies to previously inaccessible classes of receptors.
引用
收藏
页码:481 / 484
页数:4
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