荧光
化学
荧光显微镜
显微镜
DNA
全内反射荧光显微镜
纳米棒
纳米技术
分辨率(逻辑)
原位
生物物理学
生物系统
光学
生物
生物化学
计算机科学
材料科学
物理
人工智能
有机化学
作者
Chenxiang Lin,Ralf Jungmann,Andrew M. Leifer,Chao Li,Daniel Levner,George M. Church,William M. Shih,Peng Yin
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2012-09-24
卷期号:4 (10): 832-839
被引量:278
摘要
The identification and differentiation of a large number of distinct molecular species with high temporal and spatial resolution is a major challenge in biomedical science. Fluorescence microscopy is a powerful tool, but its multiplexing ability is limited by the number of spectrally distinguishable fluorophores. Here, we used (deoxy)ribonucleic acid (DNA)-origami technology to construct submicrometre nanorods that act as fluorescent barcodes. We demonstrate that spatial control over the positioning of fluorophores on the surface of a stiff DNA nanorod can produce 216 distinct barcodes that can be decoded unambiguously using epifluorescence or total internal reflection fluorescence microscopy. Barcodes with higher spatial information density were demonstrated via the construction of super-resolution barcodes with features spaced by ∼40 nm. One species of the barcodes was used to tag yeast surface receptors, which suggests their potential applications as in situ imaging probes for diverse biomolecular and cellular entities in their native environments. Life-science research and biomedical diagnostics call for robust fluorescence barcodes of compact size and high multiplexing capability. Here DNA-origami technology was used to construct a new kind of geometrically encoded barcode with excellent structural stiffness. They hold promise for both in situ and ex situ imaging of diverse biologically relevant entities.
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