4.8 Article

Scan and Unlock: A Programmable DNA Molecular Automaton for Cell-Selective Activation of Ligand-Based Signaling

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 12, Pages 6733-6743

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202015129

Keywords

cell signaling; cell-surface proteins; DNA-based chemical reaction networks; ligand– receptor interaction; logic operation

Funding

  1. National Natural Science Foundation of China [21725503, 22034002, 21575038, 21803057]

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Selective modulation of ligand-receptor interaction is crucial in targeted therapy. The SUDA system uses embedded DNA-based chemical reaction networks to scan and evaluate molecular profiles of cell-surface proteins, achieving cell-specific signal modulation by quickly unlocking the protein-ligand in proximity to the target cell-surface. The versatility of the SUDA strategy is shown through engineering TNF alpha to induce programmed cell death of target cell subpopulations.
Selective modulation of ligand-receptor interaction is essential in targeted therapy. In this study, we design an intelligent scan and unlock DNA automaton (SUDA) system to equip a native protein-ligand with cell-identity recognition and receptor-mediated signaling in a cell-type-specific manner. Using embedded DNA-based chemical reaction networks (CRNs) on the cell surface, SUDA scans and evaluates molecular profiles of cell-surface proteins via Boolean logic circuits. Therefore, it achieves cell-specific signal modulation by quickly unlocking the protein-ligand in proximity to the target cell-surface to activate its cognate receptor. As a proof of concept, we non-genetically engineered hepatic growth factor (HGF) with distinct logic SUDAs to elicit target cell-specific HGF signaling and wound healing behaviors in multiple heterogeneous cell types. Furthermore, the versatility of the SUDA strategy was shown by engineering tumor necrotic factor-alpha (TNF alpha) to induce programmed cell death of target cell subpopulations through cell-specific modulation of TNFR1 signaling.

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