Single cell kinase signaling assay using pinched flow coupled droplet microfluidics

被引:30
作者
Ramji, Ramesh [1 ]
Wang, Ming [1 ]
Bhagat, Ali Asgar S. [2 ]
Weng, Daniel Tan Shao [3 ]
Thakor, Nitish V. [1 ,4 ]
Lim, Chwee Teck [1 ,5 ]
Chen, Chia-Hung [1 ,4 ]
机构
[1] Natl Univ Singapore, Dept Biomed Engn, Singapore 117575, Singapore
[2] Clearbridge Biomed Pte Ltd, Singapore 118257, Singapore
[3] Natl Canc Ctr Singapore, Singapore 169610, Singapore
[4] Singapore Inst Neurotechnol, Singapore 117456, Singapore
[5] Natl Univ Singapore, Dept Mech Engn, Singapore 117575, Singapore
关键词
HIGH-THROUGHPUT; PROTEIN-KINASE; CAPILLARY-ELECTROPHORESIS; MAMMALIAN-CELLS; GROWTH-FACTOR; ENCAPSULATION; RECEPTOR; CANCER; ACTIVATION; VERSATILE;
D O I
10.1063/1.4878635
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Droplet-based microfluidics has shown potential in high throughput single cell assays by encapsulating individual cells in water-in-oil emulsions. Ordering cells in a micro-channel is necessary to encapsulate individual cells into droplets further enhancing the assay efficiency. This is typically limited due to the difficulty of preparing high-density cell solutions and maintaining them without cell aggregation in long channels (>5 cm). In this study, we developed a short pinched flow channel (5 mm) to separate cell aggregates and to form a uniform cell distribution in a droplet-generating platform that encapsulated single cells with >55% encapsulation efficiency beating Poisson encapsulation statistics. Using this platform and commercially available Sox substrates (8-hydroxy-5-(N, N-dimethylsulfonamido)-2-methylquinoline), we have demonstrated a high throughput dynamic single cell signaling assay to measure the activity of receptor tyrosine kinases (RTKs) in lung cancer cells triggered by cell surface ligand binding. The phosphorylation of the substrates resulted in fluorescent emission, showing a sigmoidal increase over a 12 h period. The result exhibited a heterogeneous signaling rate in individual cells and showed various levels of drug resistance when treated with the tyrosine kinase inhibitor, gefitinib. (C) 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License.
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页数:9
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