Year: 2026
Type: article
Abstract: RNA regulators offer a promising path for building complex, orthogonal circuits due to their low resource demands and design flexibility. In this study, we explore their potential as signaling molecules in communication between synthetic cells. Specifically, we engineer populations of heterogenetic porous polymer cell mimics to produce, emit, and receive two types of small synthetic RNA regulators. These RNAs are required to activate reporter expression at both the levels of transcription and translation. We distribute this AND gate circuit in receiver and two types of sender cell mimics to compare the distributed logic computation to the behavior of the circuit in well-mixed, bulk cell-free expression reactions. Analyzing different densities and spatial arrangements of senders and receivers, we reveal spatiotemporal gradients in RNA signals and identify configurations that increase specific activation. With small regulatory RNAs, the engineering toolbox for communication between synthetic cells expands to include a programmable class of signaling molecules. The rapid turnover of RNA suggests applications in establishing dynamic signaling gradients in communities of synthetic cells.
Source: ACS Synthetic Biology
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
Funder: Deutsche Forschungsgemeinschaft
Award: G7830801445
OpenAlex ID: W7124429543
