Hell Stefan W, Dyba Marcus, Jakobs Stefan
Max Planck Institute for Biophysical Chemistry, Department of NanoBiophotonics, Am Fassberg 11, 37070 Göttingen, Germany.
Curr Opin Neurobiol. 2004 Oct;14(5):599-609. doi: 10.1016/j.conb.2004.08.015.
Spatio-temporal visualization of cellular structures by fluorescence microscopy has become indispensable in biology. However, the resolution of conventional fluorescence microscopy is limited by diffraction to about 180 nm in the focal plane and to about 500 nm along the optic axis. Recently, concepts have emerged that overcome the diffraction resolution barrier fundamentally. Formed on the basis of reversible saturable optical transitions, these concepts might eventually allow us to investigate hitherto inaccessible details within live cells.
通过荧光显微镜对细胞结构进行时空可视化已成为生物学中不可或缺的手段。然而,传统荧光显微镜的分辨率受衍射限制,在焦平面上约为180纳米,沿光轴约为500纳米。最近,出现了一些从根本上克服衍射分辨率障碍的概念。这些基于可逆饱和光学跃迁形成的概念最终可能使我们能够研究活细胞内迄今无法触及的细节。