Gold Nanorod Nanolayer-Mediated Photothermal Transfection Promotes DNA Nanomachine Crossing of Cell Membranes for Sensitive Cell Imaging

The transmembrane efficiency of DNA nanomachines greatly affects the performance of cell imaging. The current transmembrane methods suffer from long time incubation, low efficiency, and potential cyto-toxicity. Here, we report on a novel gold nanorod <b>n</b>anolayer-<b>m</b>ediated <b>p</b>hotothermal <b>t</b>ransfection (AuNRs-NMPT) method to deliver a DNA nanomachine across the cell membrane. Due to good photothermal effects, AuNRs <b>n</b>anolayer-<b>f</b>unctionalized <b>s</b>lide (AuNRs-NFS) converted light energy into local heat. Local heat disrupted the fluidity of the cell membrane for perforation. The DNA nanomachine penetrates the cell membrane rapidly and efficiently via those holes under the optimal laser power and irradiation time. The AuNRs-NMPT exhibited a 12-fold lower incubation time and 13-fold higher fluorescent intensity compared to that of common direct incubation. The cells also exhibited a high cell viability after being treated with the AuNRs-NMPT, due to cell membrane self-repair. Due to efficient, rapid, and low cytotoxic transmembrane transfection, the AuNRs-NMPT ensures sensitive cell imaging of miRNA-21. The proposed AuNRs-NMPT will promote the application of DNA nanomachines for clinical cancer diagnosis in the future.

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Publication Details

Journal
Analytical Chemistry
Published
2025-02-03
DOI
https://doi.org/10.1021/acs.analchem.4c06179
Citations
4
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
3.22

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article

Gold Nanorod Nanolayer-Mediated Photothermal Transfection Promotes DNA Nanomachine Crossing of Cell Membranes for Sensitive Cell Imaging

Xiaoxuan Ning, Jiayu Wang, Yixiang Duan, Xinyu Kong et al.
4 citations
Analytical Chemistry
Advanced biosensing and bioanalysis techniques
3.22
article

Gold Nanorod Nanolayer-Mediated Photothermal Transfection Promotes DNA Nanomachine Crossing of Cell Membranes for Sensitive Cell Imaging

Xiaoxuan Ning, Jiayu Wang, Yixiang Duan, Xinyu Kong, Zewei Luo, Yanting Feng, Yu Li, Binbin Lu, Mingyue Li
article en
4 citations

Abstract

The transmembrane efficiency of DNA nanomachines greatly affects the performance of cell imaging. The current transmembrane methods suffer from long time incubation, low efficiency, and potential cyto-toxicity. Here, we report on a novel gold nanorod <b>n</b>anolayer-<b>m</b>ediated <b>p</b>hotothermal <b>t</b>ransfection (AuNRs-NMPT) method to deliver a DNA nanomachine across the cell membrane. Due to good photothermal effects, AuNRs <b>n</b>anolayer-<b>f</b>unctionalized <b>s</b>lide (AuNRs-NFS) converted light energy into local heat. Local heat disrupted the fluidity of the cell membrane for perforation. The DNA nanomachine penetrates the cell membrane rapidly and efficiently via those holes under the optimal laser power and irradiation time. The AuNRs-NMPT exhibited a 12-fold lower incubation time and 13-fold higher fluorescent intensity compared to that of common direct incubation. The cells also exhibited a high cell viability after being treated with the AuNRs-NMPT, due to cell membrane self-repair. Due to efficient, rapid, and low cytotoxic transmembrane transfection, the AuNRs-NMPT ensures sensitive cell imaging of miRNA-21. The proposed AuNRs-NMPT will promote the application of DNA nanomachines for clinical cancer diagnosis in the future.

Analytical ChemistryVol. 97(5)
Ministry of Education of the People's Republic of China (CN), Shanxi Medical University (CN), Chengdu Medical College (CN), Sichuan University (CN), Institute for Analytical Instrumentation (RU), Shanxi Fenyang Hospital (CN)
National Natural Science Foundation of China, Sichuan Province Science and Technology Support Program, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Key Research and Development Projects of Shaanxi Province
Zero hunger
Openalex Percentile: Top 9%
Advanced biosensing and bioanalysis techniques
3.22
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