期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 144, 期 4, 页码 1572-1579出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c09844
关键词
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资金
- JSPS KAKENHI [JP19K22250, JP20H02858, JP21H05025]
- PRESTO from Japan Science and Technology Agency [JPMJPR14F7, JPMJPR15F4]
- AMEDPRIME [JP21gm6210027]
- AMED [21am0401007]
- Asahi Glass Foundation
- Nakatani Foundation
This study presents a color-changing fluorescent barcode (CCFB) approach that allows for multiple labeling with a simple nucleic acid structure design. The CCFB method is easy to operate and time-saving, and has been successfully used for labeling multiple targets and detecting intracellular proteins.
Fluorescence imaging techniques have contributed to our understanding of various biological phenomenon; however, fluorescence spectral overlap significantly restricts multiplexing capability. Several strategies have been reported to overcome this limitation by utilizing the superior programmability of DNA technologies and nanostructures, but in practice, it remains challenging to achieve broad adoption of these multiplexed detection methods due to the complexities of these DNA designs. Here we report a color-changing fluorescent barcode (CCFB) approach that enables multiple labeling with simple and small nucleic acid structure design based on sequential toehold-mediated strand displacement reaction. The emission color of CCFB can vary in the predetermined sequence so that multiple targets can be detected simultaneously. The CCFB complex is composed of several oligonucleotides, and its color sequence can be easily expanded further. The CCFB approach is easy and time-saving to operate since the irreversible color-changing reaction occurs by simply adding complementary oligonucleotide. We herein developed 27 different CCFB labels, which required only 14 oligonucleotides. We demonstrated that the CCFB system can be used to label multiple targets by attaching CCFB label to polystyrene beads. Moreover, the CCFB can be used to detect intracellular proteins simultaneously when it is attached to antibodies. We expect that this practical platform will be adopted for comprehensive biomolecular imaging in cells.
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