Schmidt Roman, Wurm Christian A, Jakobs Stefan, Engelhardt Johann, Egner Alexander, Hell Stefan W
Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37077 Göttingen, Germany.
Nat Methods. 2008 Jun;5(6):539-44. doi: 10.1038/nmeth.1214. Epub 2008 May 18.
The resolution of any linear imaging system is given by its point spread function (PSF) that quantifies the blur of an object point in the image. The sharper the PSF, the better the resolution is. In standard fluorescence microscopy, however, diffraction dictates a PSF with a cigar-shaped main maximum, called the focal spot, which extends over at least half the wavelength of light (lambda = 400-700 nm) in the focal plane and >lambda along the optical axis (z). Although concepts have been developed to sharpen the focal spot both laterally and axially, none of them has reached their ultimate goal: a spherical spot that can be arbitrarily downscaled in size. Here we introduce a fluorescence microscope that creates nearly spherical focal spots of 40-45 nm (lambda/16) in diameter. Fully relying on focused light, this lens-based fluorescence nanoscope unravels the interior of cells noninvasively, uniquely dissecting their sub-lambda-sized organelles.
任何线性成像系统的分辨率由其点扩散函数(PSF)决定,该函数量化了图像中物体点的模糊程度。PSF越清晰,分辨率就越好。然而,在标准荧光显微镜中,衍射决定了PSF具有一个雪茄形的主峰,称为焦斑,其在焦平面上延伸至少半个光波长(λ = 400 - 700 nm),并且沿光轴(z)方向延伸超过λ。尽管已经开发出了在横向和轴向上锐化焦斑的概念,但它们都没有达到最终目标:一个尺寸可以任意缩小的球形光斑。在这里,我们介绍一种荧光显微镜,它能产生直径为40 - 45 nm(λ/16)的近乎球形的焦斑。这种基于透镜的荧光纳米显微镜完全依靠聚焦光,能够无创地揭示细胞内部结构,独特地剖析其亚波长尺寸的细胞器。