DNA
化学
费斯特共振能量转移
荧光
生物物理学
纳米技术
材料科学
光学
生物化学
生物
物理
作者
Qin Fu,Yicun Li,Yuheng Lv,Tenghui Ye,Xi Liu,Chenchen He,Xinchao Liu,Zi-Dong Lu,Peng Shi
标识
DOI:10.1021/acs.analchem.5c02025
摘要
The DNA-barcoding method has revolutionized immunofluorescence imaging, offering a transformative approach to protein visualization and analysis. However, achieving effective signal amplification while maintaining precise target localization remains a critical challenge. In this study, we developed fluorescent DNA-polymer conjugates through enzyme-catalysis-mediated reversible addition-fragmentation chain transfer polymerization, enabling the attachment of multiple fluorescent molecules to a single DNA strand. Utilizing a straightforward one-step DNA complementation process, DNA-polymers facilitate in situ signal amplification without the need for complex DNA nanostructures. Unlike DNA self-assembly-based amplification techniques, this approach minimizes positional deviations caused by bulky DNA structures, thereby significantly enhancing the protein localization accuracy. We validated the precision of DNA-polymers in protein localization using stochastic optical reconstruction microscopy and demonstrated their signal amplification and multiplexed imaging capabilities in expansion microscopy and peripheral blood leukocyte analysis. This versatile platform enables a broad range of fluorescence imaging applications, including signal amplification, multiplexed protein imaging, and super-resolution imaging, positioning DNA-polymers as a powerful tool with immense potential to advance diverse areas of biological research.
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