Fiolka Reto
Department of Cell Biology, UT Southwestern Medical Center, Dallas, Texas, USA.
Methods Cell Biol. 2014;123:295-313. doi: 10.1016/B978-0-12-420138-5.00016-1.
Optical microscopy enables minimally invasive imaging of cellular structures and processes with high specificity via fluorescent labeling, but its spatial resolution is fundamentally limited to approximately half the wavelength of light. Structured illumination microscopy (SIM) can improve this limit by a factor of two while keeping all advantages of light microscopy. Most importantly, SIM is compatible with live-cell imaging, as it only requires low illumination intensities and can rapidly acquire large field of views. It can also take advantage of essentially all fluorophores that are available for fluorescence microscopy and it does not require any specialized sample preparation.
光学显微镜通过荧光标记能够以高特异性对细胞结构和过程进行微创成像,但其空间分辨率从根本上限制在约为光波长的一半。结构照明显微镜(SIM)可以将这一限制提高两倍,同时保留光学显微镜的所有优点。最重要的是,SIM与活细胞成像兼容,因为它只需要低照明强度,并且能够快速获取大视野。它还可以利用基本上所有可用于荧光显微镜的荧光团,并且不需要任何特殊的样品制备。