光漂白
荧光团
扫描电镜
荧光
纳米技术
显微镜
荧光寿命成像显微镜
化学
生物物理学
荧光显微镜
单线态氧
发色团
生物成像
材料科学
DNA
DNA纳米技术
分子成像
量子点
膜
活体细胞成像
受激发射
菁
时间分辨率
微流控
DNA折纸
分子信标
光漂白后的荧光恢复
共价键
费斯特共振能量转移
作者
C. F. Liang,Q. Y. Li,Bin Chen,Tingting Zhai,Xiaoqian Luo,Yi Yang,Jiang Qian,Dan Zhao,Shihua Luo,Fei Wang,Qian Li,Jianlei Shen,Chunhai Fan
标识
DOI:10.1073/pnas.2514438123
摘要
Nanoconfinement as observed in natural (e.g. green fluorescent protein, GFP) or artificial (metal-organic or covalent organic frameworks) systems effectively modulates chemical and physical properties of encapsulated molecules for various photonic, electronic, or catalytic applications. Inspired by GFP's barrel-like peptide scaffold, which stabilizes the chromophore within a confined space, here we develop photobleaching-resistant super-resolution DNA framework (SDF) dots that enables programmable confinement of various types of fluorophores within the inner cavity resembling GFP. We find that SDF dots are resistant to reactive oxygen species-induced photobleaching due to the shielding effects of DNA frameworks. SDF dots with four fluorophores labeling inside of the cavity leads to ~1.8-fold enhancement in photostability compared to the corner labeling, whereas ~50-fold enhancement compared to single fluorophore labeled on double-stranded DNA. These ultrastable SDF dots are readily adaptable for super-resolution imaging including stimulated emission depletion (STED) and structured illumination microscopy (SIM) imaging. We realize STED imaging of live cell membranes over 30 min. We further construct ultrastable super-resolution SIM barcodes that can distinguish eighteen colored barcodes with a spatial resolution of ~70 nm. This strategy provides a versatile platform for engineering ultrastable fluorescent probes for advancing super-resolution imaging and single-particle tracking in biophysics and biomedical research.
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