Lang Marion C, Engelhardt Johann, Hell Stefan W
High Resolution Optical Microscopy Division, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Opt Lett. 2007 Feb 1;32(3):259-61. doi: 10.1364/ol.32.000259.
Practical 4Pi microscopy has so far exclusively relied on multiphoton excitation of fluorescence, because the nonlinear suppression of contributions from higher-order sidelobes was mandatory for unambiguous axial superresolution. We show that novel lenses of 74 degrees semiaperture angle enable biological 4Pi microscopy with regular one-photon fluorescence excitation, thus increasing the signal and reducing system complexity and cost. An axial resolution of 95 nm, corresponding to a more than fourfold improvement over confocal microscopy, is verified in the imaging of microtubules in mammalian cells.
实用的4Pi显微镜迄今为止完全依赖于荧光的多光子激发,因为对于明确的轴向超分辨率而言,高阶旁瓣贡献的非线性抑制是必不可少的。我们表明,半孔径角为74度的新型透镜能够通过常规的单光子荧光激发实现生物4Pi显微镜,从而增加信号并降低系统复杂性和成本。在对哺乳动物细胞中的微管成像时,验证了95纳米的轴向分辨率,这比共聚焦显微镜提高了四倍多。