Efficient multi-gene expression in cell-free droplet microreactors

Journal Article (2022)
Author(s)

Ana Maria Sierra (TU Delft - BN/Christophe Danelon Lab, King Abdullah University of Science and Technology)

Stefan T. Arold (CNRS/Université de Montpellier II, King Abdullah University of Science and Technology)

Raik Grünberg (King Abdullah University of Science and Technology)

Research Group
BN/Christophe Danelon Lab
Copyright
© 2022 A.M. Restrepo Sierra, Stefan T. Arold, Raik Grünberg
DOI related publication
https://doi.org/10.1371/journal.pone.0260420
More Info
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Publication Year
2022
Language
English
Copyright
© 2022 A.M. Restrepo Sierra, Stefan T. Arold, Raik Grünberg
Research Group
BN/Christophe Danelon Lab
Issue number
3
Volume number
17
Reuse Rights

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Abstract

Cell-free transcription and translation systems promise to accelerate and simplify the engineering of proteins, biological circuits and metabolic pathways. Their encapsulation on microfluidic platforms can generate millions of cell-free reactions in picoliter volume droplets. However, current methods struggle to create DNA diversity between droplets while also reaching sufficient protein expression levels. In particular, efficient multi-gene expression has remained elusive. We here demonstrate that co-encapsulation of DNA-coated beads with a defined cell-free system allows high protein expression while also supporting genetic diversity between individual droplets. We optimize DNA loading on commercially available microbeads through direct binding as well as through the sequential coupling of up to three genes via a solid-phase Golden Gate assembly or BxB1 integrase-based recombineering. Encapsulation with an off-the-shelf microfluidics device allows for single or multiple protein expression from a single DNA-coated bead per 14 pL droplet. We envision that this approach will help to scale up and parallelize the rapid prototyping of more complex biological systems.