A programmable and automated optical electrowetting-on-dielectric (oEWOD) driven platform for massively parallel and sequential processing of single cell assay operations
Lawrence G. WelchiD, Jasper G. EstraneroiD, Panagiotis TourlomousisiD, Robert C. R. Wootton, Valentin RaduiD, Carlos Gonzalez-FernandeziD, Tim J. PuchtleriD, Claire M. MurzeauiD, Nele M. G. DieckmanniD, Aya ShibaharaiD, Brooke W. LongbottomiD, Clare Elizabeth BryantiD, Emma L. TalbotiD
Abstract
Recently, there has been an increasing emphasis on single cell profiling for high-throughput screening workflows in drug discovery and life sciences research. However, the biology underpinning these screens is often complex and is insufficiently addressed by singleplex assay screens. Traditional single cell screening technologies have created powerful sets of omic data that allow users to bioinformatically infer biological function, but have as of yet not empowered direct functional analysis at the level of each individual cell. Consequently, screening campaigns often require multiple secondary screens leading to laborious, time-consuming and expensive workflows in which attrition points may not be queried until late in the process. We describe a platform that harnesses droplet microfluidics and optical electrowetting-on-dielectric (oEWOD) to perform highly-controlled sequential and multiplexed single cell assays in massively parallelised workflows to enable complex cell profiling during screening. Soluble reagents or objects, such as cells or assay beads, are encapsulated into droplets of media in fluorous oil and are actively filtered based on size and optical features ensuring only desirable droplets (e.g. single cell droplets) are retained for analysis, thereby overcoming the Poisson probability distribution. Droplets are stored in an array on a temperature-controlled chip and the history of individual droplets is logged from the point of filter until completion of the workflow. On chip, droplets are subject to an automated and flexible suite of operations including the merging of sample droplets and the fluorescent acquisition of assay readouts to enable complex sequential assay workflows. To demonstrate the broad utility of the platform, we present examples of single-cell functional workflows for various applications such as antibody discovery, infectious disease, and cell and gene therapy.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 15
- FWCI
- 1.43
- Field percentile
- top 20%
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Multiplexed fluorescence and scatter detection with single cell resolution using on-chip fiber optics for droplet microfluidic applications
- Droplet array-based platform for parallel optical analysis of dynamic extracellular vesicle secretion from single cells
K. Hattori, Y. Goda, … S. Ota·bioRxiv·Apr 7, 2022
- Printed Droplet Microfluidics for on demand dispensing of picoliter droplets and cells
R. H. Cole, S.-Y. Tang, … A. R. Abate·bioRxiv·Jul 21, 2017
- Real-time pooled optical screening with single-cell isolation capability.
Praneeth Karempudi, Elias Amselem, … Johan Elf·bioRxiv·Sep 21, 2023
- DropletFactory CORE - a droplet cytometry and sorting platform for fast and accessible screening in biotechnology
Veere Robin, Merle N. Zenner, … Ott Scheler·bioRxiv·Mar 12, 2026
- Droplet microfluidics forward for tracing target cells at single-cell transcriptome resolution