化学
适体
核糖核酸
活体细胞成像
单元格排序
荧光
荧光寿命成像显微镜
纳米技术
生物物理学
罗丹明
计算生物学
正交性
分子成像
核酸结构
DNA
光学成像
小RNA
动态成像
分类
细胞
作者
Simon Fürbacher,Pia Doll,JingYe Zhang,Laura Lange,Niklas van den Bergh,Yaqing Zhang,Erika Vitiello,Franziska Grün,Murat Sunbul,Andres Jäschke
摘要
Despite their advantageous properties for live-cell imaging and super-resolution microscopy, high-performance silicon rhodamine (SiR) near-infrared (NIR) probes are still rarely employed in RNA imaging via fluorescent light-up aptamers (FLAPs). Here, we developed the SiRiuS:SiR-5 system through a combined evolutionary approach: evolving the aptamer via fluorescence-activated cell sorting (FACS), along with targeted mutations, truncations, and rational design, and improvement of the dye by systematic chemical derivatization. This resulted in an aptamer:dye pair with high fluorogenicity and photostability, specifically optimized for visualization of RNAs in mammalian live cells. Our system demonstrates strong fluorescence enhancement in live-cell imaging, enabling time-resolved imaging of dynamic processes such as stress-granule formation. Notably, we validate its application in STED super-resolution microscopy, establishing it as a powerful NIR imaging platform for RNA structures below the diffraction limit. Its orthogonality to existing FLAPs operating in the yellow-orange spectrum further broadens its versatility for exploring complex RNA dynamics in live cells.
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