Chromatin Labeling and Imaging group, Department of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077, Göttingen, Germany.
Department of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077, Göttingen, Germany.
Nat Commun. 2023 Mar 9;14(1):1306. doi: 10.1038/s41467-023-36913-2.
The development of live-cell fluorescence nanoscopy is powered by the availability of suitable fluorescent probes. Rhodamines are among the best fluorophores for labeling intracellular structures. Isomeric tuning is a powerful method for optimizing the biocompatibility of rhodamine-containing probes without affecting their spectral properties. An efficient synthesis pathway for 4-carboxyrhodamines is still lacking. We present a facile protecting-group-free 4-carboxyrhodamines' synthesis based on the nucleophilic addition of lithium dicarboxybenzenide to the corresponding xanthone. This approach drastically reduces the number of synthesis steps, expands the achievable structural diversity, increases overall yields and permits gram-scale synthesis of the dyes. We synthesize a wide range of symmetrical and unsymmetrical 4-carboxyrhodamines covering the whole visible spectrum and target them to multiple structures in living cells - microtubules, DNA, actin, mitochondria, lysosomes, Halo-tagged and SNAP-tagged proteins. The enhanced permeability fluorescent probes operate at submicromolar concentrations, allowing high-contrast STED and confocal microscopy of living cells and tissues.
活细胞荧光纳米显微镜的发展依赖于合适的荧光探针的可用性。若丹明是标记细胞内结构的最佳荧光团之一。同系物调谐是一种在不影响其光谱特性的情况下优化含若丹明探针生物相容性的有效方法。目前仍然缺乏有效的 4-羧基若丹明合成途径。我们提出了一种简便的无保护基 4-羧基若丹明的合成方法,基于羧酸二苯锂对相应呫吨酮的亲核加成。这种方法大大减少了合成步骤的数量,扩展了可实现的结构多样性,提高了总收率,并允许染料的克级规模合成。我们合成了广泛的对称和非对称的 4-羧基若丹明,涵盖整个可见光谱,并将其靶向到活细胞中的多种结构 - 微管、DNA、肌动蛋白、线粒体、溶酶体、 Halo 标记和 SNAP 标记蛋白。增强通透性荧光探针在亚毫摩尔浓度下工作,允许对活细胞和组织进行高对比度 STED 和共聚焦显微镜观察。