适体
扫描电镜
荧光
活体细胞成像
罗丹明
核糖核酸
生物物理学
荧光寿命成像显微镜
分子成像
显微镜
化学
超分辨率
纳米技术
细胞
生物
材料科学
分子生物学
物理
光学
计算机科学
生物化学
遗传学
体内
人工智能
图像(数学)
基因
作者
Daniel Englert,Eva‐Maria Burger,Franziska Grün,Mrigank Singh Verma,Jens Lackner,Marko Lampe,Bastian Bühler,Janin Schokolowski,G. Ulrich Nienhaus,Andres Jäschke,Murat Sünbül
标识
DOI:10.1038/s41467-023-39611-1
摘要
Live-cell RNA imaging with high spatial and temporal resolution remains a major challenge. Here we report the development of RhoBAST:SpyRho, a fluorescent light-up aptamer (FLAP) system ideally suited for visualizing RNAs in live or fixed cells with various advanced fluorescence microscopy modalities. Overcoming problems associated with low cell permeability, brightness, fluorogenicity, and signal-to-background ratio of previous fluorophores, we design a novel probe, SpyRho (Spirocyclic Rhodamine), which tightly binds to the RhoBAST aptamer. High brightness and fluorogenicity is achieved by shifting the equilibrium between spirolactam and quinoid. With its high affinity and fast ligand exchange, RhoBAST:SpyRho is a superb system for both super-resolution SMLM and STED imaging. Its excellent performance in SMLM and the first reported super-resolved STED images of specifically labeled RNA in live mammalian cells represent significant advances over other FLAPs. The versatility of RhoBAST:SpyRho is further demonstrated by imaging endogenous chromosomal loci and proteins.
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