Hell S W, Booth M, Wilms S, Schnetter C M, Kirsch A K, Arndt-Jovin D J, Jovin T M
High Resolution Optical Microscopy Group, Max Planck Institute for Biophysical Chemistry, D-37070 Göttingen, Germany.
Opt Lett. 1998 Aug 1;23(15):1238-40. doi: 10.1364/ol.23.001238.
We report on scanning far- and near-field two-photon microscopy of cell nuclei stained with DAPI and bisbenzimidazole Hoechst 33342 (BBI-342) with the 647-nm laser line of a cw ArKr mixed-gas laser. Two-photon-excited fluorescence images are obtained for 50-200 mW of average power at the sample. A nearly quadratic dependence of fluorescence intensity on laser power confirmed the two-photon effect. The nonlinearity was further supported by evidence of three-dimensional sectioning in a scanning far-field microscope. We find that the cw two-photon irradiation sufficient for imaging within typically 5 s does not significantly impair cell cycling of BBI-342-labeled live cells. Finally, high-resolution imaging in scanning near-field microscopy with good contrast is demonstrated.
我们报告了使用连续波氩氪混合气体激光器的647纳米激光线,对用4',6-二脒基-2-苯基吲哚(DAPI)和双苯并咪唑Hoechst 33342(BBI-342)染色的细胞核进行扫描远场和近场双光子显微镜观察的结果。在样品处平均功率为50-200毫瓦的情况下获得了双光子激发荧光图像。荧光强度对激光功率的近似二次依赖性证实了双光子效应。扫描远场显微镜中的三维切片证据进一步支持了这种非线性。我们发现,在通常5秒内足以进行成像的连续波双光子照射不会显著损害BBI-342标记的活细胞的细胞周期。最后,展示了在扫描近场显微镜中具有良好对比度的高分辨率成像。