High‐Resolution Patterned Delivery of Chemical Signals From 3D‐Printed Picoliter Droplet Networks

J Jorin Riexinger (Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK) T Thomas Caganek (Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK) X Xingzao Wang (Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK) Y Yutong Yin K Khoa Chung (Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK) L Linna Zhou H Hagan Bayley (Department of Chemistry, University of Oxford, Mansfield Road, OX1 3TA Oxford, U.K.) R Ravinash Krishna Kumar (Section of Structural and Synthetic Biology Department of Infectious Disease Imperial College London Sir Alexander Fleming Building, Imperial College Road London SW7 2AZ UK)

Abstract

Abstract Synthetic cells, such as giant unilamellar vesicles, can be engineered to detect and release chemical signals to control target cell behavior. However, control over the targeting of cell populations is limited due to poor spatial or temporal resolution and the inability of synthetic cells to deliver patterned signals. Here, 3D‐printed picoliter droplet networks are described that direct gene expression in underlying bacterial populations by patterned release of a chemical signal with temporal control. Shrinkage of the droplet networks prior to use achieves spatial control over gene expression with ≈50 µm resolution. Ways to store chemical signals in the droplet networks and to activate release at controlled points in time are also demonstrated. Finally, it is shown that the spatially‐controlled delivery system can regulate competition between bacteria by inducing the patterned expression of toxic bacteriocins. This system provides the groundwork for the use of picoliter droplet networks in fundamental biology and in medicine in applications that require the controlled formation of chemical gradients (i.e., for the purpose of local control of gene expression) within a target group of cells.

Article Details

Volume / Issue Vol. 37, Issue 28
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (8)

J

Jorin Riexinger

Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK

T

Thomas Caganek

Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK

X

Xingzao Wang

Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK

Y

Yutong Yin

K

Khoa Chung

Chemistry Research Laboratory Department of Chemistry University of Oxford 12 Mansfield Road Oxford OX1 3TA UK

L

Linna Zhou

H

Hagan Bayley

Department of Chemistry, University of Oxford, Mansfield Road, OX1 3TA Oxford, U.K.

R

Ravinash Krishna Kumar

Section of Structural and Synthetic Biology Department of Infectious Disease Imperial College London Sir Alexander Fleming Building, Imperial College Road London SW7 2AZ UK