Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Furo, Chikusa, Nagoya 464-8602 (Japan).
Department of Chemistry, Graduate School of Science, Nagoya University, Furo, Chikusa, Nagoya 464-8602 (Japan).
Angew Chem Int Ed Engl. 2015 Dec 7;54(50):15213-7. doi: 10.1002/anie.201507939. Epub 2015 Oct 23.
The development of stimulated emission depletion (STED) microscopy represented a major breakthrough in cellular and molecular biology. However, the intense laser beams required for both excitation and STED usually provoke rapid photobleaching of fluorescent molecular probes, which significantly limits the performance and practical utility of STED microscopy. We herein developed a photoresistant fluorescent dye C-Naphox as a practical tool for STED imaging. With excitation using either a λ=405 or 488 nm laser in protic solvents, C-Naphox exhibited an intense red/orange fluorescence (quantum yield ΦF >0.7) with a large Stokes shift (circa 5900 cm(-1) ). Even after irradiation with a Xe lamp (300 W, λex =460 nm, full width at half maximum (FWHM)=11 nm) for 12 hours, 99.5 % of C-Naphox remained intact. The high photoresistance of C-Naphox allowed repeated STED imaging of HeLa cells. Even after recording 50 STED images, 83 % of the initial fluorescence intensity persisted.
受激发射耗散(STED)显微镜的发展代表了细胞和分子生物学的重大突破。然而,激发和 STED 所需的强激光束通常会导致荧光分子探针迅速光漂白,这极大地限制了 STED 显微镜的性能和实际应用。我们在此开发了一种耐光荧光染料 C-Naphox,作为 STED 成像的实用工具。在质子溶剂中使用 λ=405 或 488nm 的激光进行激发时,C-Naphox 表现出强烈的红/橙色荧光(量子产率 ΦF>0.7),具有较大的斯托克斯位移(约 5900cm(-1))。即使在用 Xe 灯(300W,λex=460nm,半峰全宽(FWHM)=11nm)照射 12 小时后,C-Naphox 的 99.5%仍保持完整。C-Naphox 的高耐光性允许对 HeLa 细胞进行重复的 STED 成像。即使在记录 50 个 STED 图像后,初始荧光强度仍保持 83%。