Ratiometric Detection of Zn2+ Using DNAzyme-Based Bioluminescence Resonance Energy Transfer Sensors

Author:

Wu Yuting12ORCID,Lewis Whitney12ORCID,Wai Jing Luen23ORCID,Xiong Mengyi24,Zheng Jiao2,Yang Zhenglin15ORCID,Gordon Chloe1,Lu Ying1ORCID,New Siu Yee3ORCID,Zhang Xiao-Bing4,Lu Yi125ORCID

Affiliation:

1. Department of Chemistry, University of Texas at Austin, Austin, TX 78712, USA

2. Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA

3. School of Pharmacy, Faculty of Science and Engineering, University of Nottingham Malaysia, Semenyih 43500, Selangor, Malaysia

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

5. Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA

Abstract

While fluorescent sensors have been developed for monitoring metal ions in health and diseases, they are limited by the requirement of an excitation light source that can lead to photobleaching and a high autofluorescence background. To address these issues, bioluminescence resonance energy transfer (BRET)-based protein or small molecule sensors have been developed; however, most of them are not highly selective nor generalizable to different metal ions. Taking advantage of the high selectivity and generalizability of DNAzymes, we report herein DNAzyme-based ratiometric sensors for Zn2+ based on BRET. The 8-17 DNAzyme was labeled with luciferase and Cy3. The proximity between luciferase and Cy3 permitted BRET when coelenterazine, the substrate for luciferase, was introduced. Adding samples containing Zn2+ resulted in a cleavage of the substrate strand, causing dehybridization of the DNAzyme construct, thus increasing the distance between Cy3 and luciferase and changing the BRET signals. Using these sensors, we detected Zn2+ in serum samples and achieved Zn2+ detection with a smartphone camera. Moreover, since the BRET pair is not the component that determines the selectivity of the sensors, this sensing platform has the potential to be adapted for the detection of other metal ions with other metal-dependent DNAzymes.

Funder

National Institutes of Health

Robert A. Welch Foundation

National Key R&D Program of China

National Natural Science Foundation of China

National Postdoctoral Program for Innovative Talents

Publisher

MDPI AG

Subject

Organic Chemistry,Inorganic Chemistry,Electrochemistry,Chemistry (miscellaneous)

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