Fluorescent Droplet Cytometry for On-Cell Phenotype Tracking

被引:14
|
作者
Yang, Xiaolong [1 ]
Liu, Wenhan [2 ]
Chan, Darren Chi-Hang [1 ]
Ahmed, Sharif U. [1 ]
Wang, Hansen [1 ]
Wang, Zongjie [3 ,4 ]
Nemr, Carine R. [5 ]
Kelley, Shana O. [6 ,7 ]
机构
[1] Univ Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON M5S 3M2, Canada
[2] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3G9, Canada
[3] Univ Toronto, Edward S Rogers Sr Dept Elect & Comp Engn, Toronto, ON M5S 3G4, Canada
[4] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3G4, Canada
[5] Univ Toronto, Fac Arts & Sci, Dept Chem, Toronto, ON M5S 3H4, Canada
[6] Univ Toronto, Dept Pharmaceut Sci, Leslie Dan Fac Pharm, Inst Biomat & Biomed Engn, Toronto, ON M5S 3M2, Canada
[7] Univ Toronto, Dept Chem, Fac Arts & Sci, Toronto, ON M5S 3M2, Canada
关键词
Cancer cells - Chemical detection - Diseases - Fluorescence - Drops - Cytology;
D O I
10.1021/jacs.0c05276
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Profiling the heterogeneous phenotypes of live cancer cells is a key capability that requires single-cell analysis. However, acquiring information at the single-cell level for live cancer cells is challenging when small collections of cells are being targeted. Here, we report single-cell analysis for low abundance cells enabled by fluorescent droplet cytometry (FDC), an approach that uses a biomarker-specific enzymatic fluorescent assay carried out using a droplet microfluidic platform. FDC utilizes DNA-functionalized antibodies in droplets to achieve specific on-cell target detection and enables characterization and profiling of live cancer cells with single-cell resolution based on their surface phenotype. Using this approach, we achieve live-cell phenotypic profiling of multiple surface markers acquired with small (<40 cells) collections of cells.
引用
收藏
页码:14805 / 14809
页数:5
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