Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37070 Göttingen (Germany), Fax: (+49) 551 201-2505; Equal contributions.
Chemphyschem. 2014 Mar 17;15(4):655-63. doi: 10.1002/cphc.201301016. Epub 2014 Jan 21.
Up to now, all demonstrations of reversible saturable optical fluorescence transitions (RESOLFT) superresolution microscopy of living cells have relied on the use of reversibly switchable fluorescent proteins (RSFP) emitting in the green spectral range. Here we show RESOLFT imaging with rsCherryRev1.4, a new red-emitting RSFP enabling a spatial resolution up to four times higher than the diffraction barrier. By co-expressing green and red RSFPs in living cells we demonstrate two-color RESOLFT imaging both for single ("donut") beam scanning and for parallelized versions of RESOLFT nanoscopy where an array of >23,000 "donut-like" minima are scanned simultaneously.
到目前为止,所有活细胞的可饱和光学荧光跃迁(RESOLFT)超分辨率显微镜的演示都依赖于使用在绿色光谱范围内发射的可逆开关荧光蛋白(RSFP)。在这里,我们展示了 rsCherryRev1.4 的 RESOLFT 成像,这是一种新的红色发射 RSFP,能够实现比衍射障碍高四倍的空间分辨率。通过在活细胞中共表达绿色和红色 RSFPs,我们证明了双色 RESOLFT 成像可用于单(“甜甜圈”)光束扫描以及 RESOLFT 纳米显微镜的并行版本,其中同时扫描了 >23,000 个“甜甜圈状”极小值的阵列。