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One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation.

Authors: Samlali KAhmadi FQuach ABVSoffer GShih SCC


Affiliations

1 Department of Electrical and Computer Engineering, Concordia University, Montréal, Québec, H3G 1M8, Canada.
2 Centre for Applied Synthetic Biology, Concordia University, Montréal, Québec, H4B 1R6, Canada.
3 Department of Biology, Concordia University, Montréal, Québec, H4B 1R6, Canada.

Description

One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation.

Small. 2020 Jul 23;:e2002400

Authors: Samlali K, Ahmadi F, Quach ABV, Soffer G, Shih SCC

Abstract

Generating a stable knockout cell line is a complex process that can take several months to complete. In this work, a microfluidic method that is capable of isolating single cells in droplets, selecting successful edited clones, and expansion of these isoclones is introduced. Using a hybrid microfluidics method, droplets in channels can be individually addressed using a co-planar electrode system. In the hybrid microfluidics device, it is shown that single cells can be trapped and subsequently encapsulate them on demand into pL-sized droplets. Furthermore, droplets containing single cells are either released, kept in the traps, or merged with other droplets by the application of an electric potential to the electrodes that is actuated through an in-house user interface. This high precision control is used to successfully sort and recover single isoclones to establish monoclonal cell lines, which is demonstrated with a heterozygous NCI-H1299 lung squamous cell population resulting from loss-of-function eGFP and RAF1 gene knockout transfections.

PMID: 32705796 [PubMed - as supplied by publisher]


Keywords: digital microfluidicsdroplet microfluidicsgene-editingsingle-celltransfection


Links

PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32705796

DOI: 10.1002/smll.202002400