DNAzymes-Embedded Framework Nucleic Acids (FNAzymes) for Metal Ions Imaging in Living Cells

Author:

Zhu Dan1,Huang Jiaxuan1,Xia Yanting1,Su Shao1ORCID,Zuo Xiaolei23,Li Qian2,Wang Lianhui1

Affiliation:

1. State Key Laboratory of Organic Electronics and Information Displays & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), Nanjing University of Posts and Telecommunications, Nanjing 210023, China

2. School of Chemistry and Chemical Engineering, National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai 200240, China

3. Shanghai Key Laboratory for Nucleic Acids Chemistry and Nanomedicine, Institute of Molecular Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China

Abstract

Simultaneous and non-destructive quantitative detection of intracellular metal ions holds great promise for improving the accuracy of diagnosis and biological research. Herein, novel multicolor DNAzymes-embedded framework nucleic acids (FNAzymes) were presented, which can easily enter cells and achieve simultaneous and quantitative detection of intracellular physiologically related Cu2+ and Zn2+. Two types of DNAzymes, specific to Cu2+ and Zn2+, were encoded in the framework nucleic acids (FNAs) via self-assembly. With the formation of a well-ordered FNAzyme nanostructure, the fluorophore and the quencher were close to each other; therefore, the fluorescence was quenched. In the presence of Cu2+ and Zn2+, the integrated FNAzymes would be specifically cleaved, resulting in the release of fluorophores in cells. Consequently, the fluorescence in living cells could be observed by a confocal microscope and semi-quantitatively analyzed by flow cytometry with low-nanomolar sensitivity for both metal ions. The FNAzymes have high uniformity and structural accuracy, which are beneficial for intracellular detection with excellent reproducibility. This proposed method offers new opportunities for non-destructive, semi-quantitative, multi-target detection in living cells.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

“Belt and Road” Innovation Cooperation Project of Jiangsu

Qinglan Project of Jiangsu Province of China

Young Scientific and Technological Talents Project of Jiangsu Association

Nanjing University of Posts and Telecommunications

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Analytical Chemistry

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