Department of Engineering Science, University of Oxford Parks Road, Oxford OX13PJ, United Kingdom.
J Microsc. 2010 Jan;237(1):103-9. doi: 10.1111/j.1365-2818.2009.03317.x.
In conventional microscopes, fluorescence emission is separated from the backscattered illumination using the Stokes shift, whereby the emission occurs at a longer wavelength to the excitation. Such separation is usually achieved through a combination of wavelength filters that divide the spectrum into mutually exclusive excitation and emission bands. It is therefore impossible in these microscopes to access the full excitation/emission spectrum of the specimen in a single image. We report on a microscope that acquired fluorescence images using illumination across the spectral range 450-680 nm; the full emission spectrum was detected simultaneously across the same range. The microscope was also combined with structured illumination optical sectioning to give three-dimensionally resolved images with improved background rejection. Full spectrum fluorescence images of biological specimens are demonstrated. As this system is more versatile than the standard fluorescence microscope, it could be of benefit in many fluorescence imaging applications.
在传统显微镜中,荧光发射通过斯托克斯位移与反向散射照明分离,其中发射发生在比激发更长的波长处。这种分离通常通过组合波长滤波器来实现,这些滤波器将光谱分成相互排斥的激发和发射带。因此,在这些显微镜中,不可能在单个图像中获得标本的完整激发/发射光谱。我们报告了一种显微镜,它使用 450-680nm 范围内的照明获取荧光图像;同时在相同范围内检测整个发射光谱。该显微镜还与结构照明光学切片相结合,给出了具有改进背景抑制的三维分辨图像。展示了生物样本的全光谱荧光图像。由于该系统比标准荧光显微镜更通用,因此它可能在许多荧光成像应用中受益。