Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120, Heidelberg, Germany.
Institute of Chemical Sciences and Engineering (ISIC), École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Nat Commun. 2019 Oct 8;10(1):4580. doi: 10.1038/s41467-019-12480-3.
Photoactivatable fluorophores are important for single-particle tracking and super-resolution microscopy. Here we present a photoactivatable fluorophore that forms a bright silicon rhodamine derivative through a light-dependent protonation. In contrast to other photoactivatable fluorophores, no caging groups are required, nor are there any undesired side-products released. Using this photoactivatable fluorophore, we create probes for HaloTag and actin for live-cell single-molecule localization microscopy and single-particle tracking experiments. The unusual mechanism of photoactivation and the fluorophore's outstanding spectroscopic properties make it a powerful tool for live-cell super-resolution microscopy.
光活化荧光团对于单粒子追踪和超分辨率显微镜非常重要。在这里,我们介绍了一种光活化荧光团,它通过光依赖性质子化形成明亮的硅罗丹明衍生物。与其他光活化荧光团不同,不需要使用笼形基团,也不会释放任何不需要的副产物。使用这种光活化荧光团,我们为 HaloTag 和肌动蛋白创建了探针,用于活细胞单分子定位显微镜和单粒子追踪实验。光活化的不寻常机制和荧光团出色的光谱特性使其成为活细胞超分辨率显微镜的强大工具。