Light‐Responsive DNA Droplets for Controlling Enzyme Cascade Pathways by Dynamic Phase Separation

S Shaohong Zhou (State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China) X Xiuqin Ju (State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China) H Hui Chen Y Yanwen Zhang (State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China) J Jing Zheng K Kemin Wang (State Key Laboratory of Chemo and Biosensing, College of Biology, College of Chemistry and Chemical Engineering) X Xiaohai Yang (State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China) J Jianbo Liu

Abstract

Abstract Precise control of enzymatic cascade pathways is essential for deepening our understanding of metabolic processes and designing synthetic biochemical systems. In this study, we present a novel approach to modulate these cascades using light‐responsive DNA droplets. Y‐motif sequences with azobenzene‐modified sticky ends (SE) were designed to form DNA droplets via liquid–liquid phase separation. These droplets enable selective sequestration of enzymes within compartments, allowing dynamic regulation of enzymatic cascades in response to ultraviolet (UV) and visible (vis) light stimuli. As a model system, we employed an incompatible enzymatic cascade, involving glucose oxidase (GOx), horseradish peroxidase (HRP), and catalase (CAT). Under visible light, the DNA droplets co‐localize enzymes within the compartments, effectively regulating metabolic flux without altering the total enzyme concentration. Upon UV exposure, the droplets disassemble, releasing the sequestered enzymes and altering cascade dynamics. The versatility of this approach was further demonstrated using an alternative enzymatic cascade system comprising galactose oxidase (GAO), myeloperoxidase (MPO), and CAT. This system demonstrates that light‐responsive DNA droplets are a powerful tool for regulating enzymatic pathways, with potential applications in synthetic biology, microreactor design, and bioengineering.

Article Details

Volume / Issue Vol. 64, Issue 31
Published July 28, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

S

Shaohong Zhou

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China

X

Xiuqin Ju

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China

H

Hui Chen

Y

Yanwen Zhang

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China

J

Jing Zheng

K

Kemin Wang

State Key Laboratory of Chemo and Biosensing, College of Biology, College of Chemistry and Chemical Engineering

X

Xiaohai Yang

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio‐Nanotechnology and Molecular Engineering of Hunan Province Hunan University Changsha 410082 P.R. China

J

Jianbo Liu