Issue 17, 2021

Dual dean entrainment with volume ratio modulation for efficient droplet co-encapsulation: extreme single-cell indexing

Abstract

The future of single cell diversity screens involves ever-larger sample sizes, dictating the need for higher throughput methods with low analytical noise to accurately describe the nature of the cellular system. Current approaches are limited by the Poisson statistic, requiring dilute cell suspensions and associated losses in throughput. In this contribution, we apply Dean entrainment to both cell and bead inputs, defining different volume packets to effect efficient co-encapsulation. Volume ratio scaling was explored to identify optimal conditions. This enabled the co-encapsulation of single cells with reporter beads at rates of ∼1 million cells per hour, while increasing assay signal-to-noise with cell multiplet rates of ∼2.5% and capturing ∼70% of cells. The method, called Pirouette coupling, extends our capacity to investigate biological systems.

Graphical abstract: Dual dean entrainment with volume ratio modulation for efficient droplet co-encapsulation: extreme single-cell indexing

Supplementary files

Article information

Article type
Paper
Submitted
06 Apr 2021
Accepted
21 Jun 2021
First published
30 Jun 2021
This article is Open Access
Creative Commons BY license

Lab Chip, 2021,21, 3378-3386

Dual dean entrainment with volume ratio modulation for efficient droplet co-encapsulation: extreme single-cell indexing

J. Harrington, L. B. Esteban, J. Butement, A. F. Vallejo, S. I. R. Lane, B. Sheth, M. S. A. Jongen, R. Parker, P. S. Stumpf, R. C. G. Smith, B. D. MacArthur, M. J. J. Rose-Zerilli, M. E. Polak, T. Underwood and J. West, Lab Chip, 2021, 21, 3378 DOI: 10.1039/D1LC00292A

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