Multi-step processing of single cells using semi-permeable capsules

Droplet microfluidics technology provides a powerful approach to isolate and process millions of single cells simultaneously. Despite many exciting applications that have emerged based on this technology, workflows based on multi-step operations, including molecular biology and cell-based phenotypic...

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Bibliographic Details
Published inLab on a chip Vol. 2; no. 21; pp. 452 - 462
Main Authors Leonaviciene, Greta, Leonavicius, Karolis, Meskys, Rolandas, Mazutis, Linas
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 27.10.2020
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Summary:Droplet microfluidics technology provides a powerful approach to isolate and process millions of single cells simultaneously. Despite many exciting applications that have emerged based on this technology, workflows based on multi-step operations, including molecular biology and cell-based phenotypic screening assays, cannot be easily adapted to droplet format. Here, we present a microfluidics-based technique to isolate single cells, or biological samples, into semi-permeable hydrogel capsules and perform multi-step biological workflows on thousands to millions of individual cells simultaneously. The biochemical reactions are performed by changing the aqueous buffer surrounding the capsules, without needing sophisticated equipment. The semi-permeable nature of the capsules' shell retains large encapsulated biomolecules (such as genome) while allowing smaller molecules (such as proteins) to passively diffuse. In contrast to conventional hydrogel bead assays, the approach presented here improves bacterial cell retention during multi-step procedures as well as the efficiency of biochemical reactions. We showcase two examples of capsule use for single genome amplification of bacteria, and expansion of individual clones into isogenic microcolonies for later screening for biodegradable plastic production. Semi-permeable capsules offers a powerful approach to isolate and process thousands of single bacterial cells simultaneously.
Bibliography:10.1039/d0lc00660b
Electronic supplementary information (ESI) available: ESI Fig. S1-S13, ESI Video S1, ESI Note. See DOI
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ISSN:1473-0197
1473-0189
DOI:10.1039/d0lc00660b