Tethered Fluorogen Assay to Visualize Membrane Apposition in Living Cells

被引:11
作者
Ackerman, Daniel S. [1 ,3 ]
Vasilev, Kalin V. [1 ,3 ]
Schmidt, Brigitte F. [2 ,3 ]
Cohen, Lianne B. [1 ,4 ]
Jarvik, Jonathan W. [1 ,3 ]
机构
[1] Carnegie Mellon Univ, Dept Biol Sci, 4400 Fifth Ave, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Chem, 4400 Fifth Ave, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Mol Biosensor & Imaging Ctr, 4400 Fifth Ave, Pittsburgh, PA 15213 USA
[4] Univ Calif San Diego, Sect Cell & Dev Biol, Div Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
MAMMALIAN SYNAPTIC CONNECTIVITY; ACTIVATING-PROTEINS; SURFACE PROTEINS; MICROSCOPY; DYES; BIOSENSORS; CONTACTS; DOMAINS; LIGHT;
D O I
10.1021/acs.bioconjchem.7b00047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe proof-of-concept for a novel approach for visualizing regions of close apposition between the surfaces of living cells. A membrane-anchored protein with high affinity for a chemical ligand is expressed on the surface of one set of cells, and the cells are co-cultured with a second set of cells that express a membrane-anchored fluorogen-activating protein (FAP). The co-cultured cells are incubated with a bivalent reagent composed of fluorogen linked to the high-affinity ligand, with the concentration of the bivalent reagent chosen to be less than the binding constant for the FAP-fluorogen pair but greater than the binding constant for the ligand-high-affinity protein pair. In these conditions, strong FAP signal is observed only in regions of close proximity between membranes of the two classes of cell, where high local concentration of fluorogen favors binding to the FAP.
引用
收藏
页码:1356 / 1362
页数:7
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