Author
Listed:
- Yang Xiao
(Nanjing University of Science and Technology)
- Longyi Zhu
(Nanjing University of Science and Technology)
- Songyuan Du
(Nanjing University of Science and Technology
Nanjing University of Science and Technology)
- Xinyi Ge
(Nanjing University of Science and Technology
Nanjing University of Science and Technology)
- Lequn Ma
(Nanjing University of Science and Technology)
- Shengyuan Deng
(Nanjing University of Science and Technology)
- Kewei Ren
(Nanjing University of Science and Technology)
Abstract
Mitochondria-lysosome interactions are critical for maintaining cellular homeostasis. Although genetically encoded protein based optogenetic technique is developed to regulate such interactions, it still suffers from shortcomings including complicated operation and potential interference to organelle functions. Here, we present a fast, simple, biocompatible and programmable platform via activable DNA regulators to achieve spatiotemporal regulation of mitochondria-lysosome interactions in living cells. In our system, two locked DNA regulators, OK-MLIR and DK-MLIR, that can be respectively activated with UV light (One Key) as well as UV light and endogenous glutathione (Dual Keys), are modularly designed for modulating mitochondria-lysosome contacts. We show that these DNA regulators can be used for facilitating mitochondrial fission and autophagy. Moreover, the DK-MLIR enables selective and efficient manipulation of target cell migration and proliferation with highly temporal and spatial controllability. This programmable and modular design principle provides a platform for organelle interaction study, cellular regulation and precision therapy.
Suggested Citation
Yang Xiao & Longyi Zhu & Songyuan Du & Xinyi Ge & Lequn Ma & Shengyuan Deng & Kewei Ren, 2025.
"Dual-key cooperatively activated DNA regulator for controlling mitochondria-lysosome interactions,"
Nature Communications, Nature, vol. 16(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63040-x
DOI: 10.1038/s41467-025-63040-x
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