A Semisynthetic Bioluminescence Sensor for Ratiometric Imaging of Metal Ions In Vivo Using DNAzymes Conjugated to An Engineered Nano‐Luciferase

Author:

Xiong Mengyi1ORCID,Wu Yuting2ORCID,Kong Gezhi1,Lewis Whitney2ORCID,Yang Zhenglin2ORCID,Zhang Hanxiao3,Xu Li1,Liu Ying1,Liu Qin1,Zhao Xuhua3,Zhang Xiao‐Bing1,Lu Yi2ORCID

Affiliation:

1. Molecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University 410082 Changsha Hunan P. R. China

2. Department of Chemistry University of Texas at Austin 78712 Austin TX USA

3. Department of Biochemistry and Molecular Biology Shanxi Medical University 030001 Taiyuan Shanxi P. R. China

Abstract

AbstractDNA‐based probes have gained significant attention as versatile tools for biochemical analysis, benefiting from their programmability and biocompatibility. However, most existing DNA‐based probes rely on fluorescence as the signal output, which can be problematic due to issues like autofluorescence and scattering when applied in complex biological materials such as living cells or tissues. Herein, we report the development of bioluminescent nucleic acid (bioLUNA) sensors that offer laser excitation‐independent and ratiometric imaging of the target in vivo. The system is based on computational modelling and mutagenesis investigations of a genetic fusion between circular permutated Nano‐luciferase (NLuc) and HaloTag, enabling the conjugation of the protein with a DNAzyme. In the presence of Zn2+, the DNAzyme sensor releases the fluorophore‐labelled strand, leading to a reduction in bioluminescent resonance energy transfer (BRET) between the luciferase and fluorophore. Consequently, this process induces ratiometric changes in the bioluminescent signal. We demonstrated that this bioLUNA sensor enabled imaging of both exogenous Zn2+ in vivo and endogenous Zn2+ efflux in normal epithelial prostate and prostate tumors. This work expands the DNAzyme sensors to using bioluminescence and thus has enriched the toolbox of nucleic acid sensors for a broad range of biomedical applications.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Postdoctoral Research Foundation of China

National Postdoctoral Program for Innovative Talents

National Institute of General Medical Sciences

Publisher

Wiley

Subject

General Chemistry,Catalysis

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