Yan Long, Rueden Curtis T, White John G, Eliceiri Kevin W
Laboratory for Optical and Computational Instrumentation, University of Wisconsin-Madison, Madison, WI, USA.
Biotechniques. 2006 Sep;41(3):249, 251, 253 passim. doi: 10.2144/000112251.
Live cell imaging has been greatly advanced by the recent development of new fluorescence microscopy-based methods such as multiphoton laser-scanning microscopy, which can noninvasively image deep into live specimens and generate images of extrinsic and intrinsic signals. Of recent interest has been the development of techniques that can harness properties of fluorescence, other than intensity, such as the emission spectrum and excited state lifetime of a fluorophore. Spectra can be used to discriminate between fluorophores, and lifetime can be used to report on the microenvironment of fluorophores. We describe a novel technique-combined spectral and lifetime imaging-which combines the benefits of multiphoton microscopy, spectral discrimination, and lifetime analysis and allows for the simultaneous collection of all three dimensions of data along with spatial and temporal information.
基于新的荧光显微镜技术(如多光子激光扫描显微镜)的最新发展,活细胞成像取得了巨大进展。多光子激光扫描显微镜可以对活标本进行非侵入性的深度成像,并生成外部和内部信号的图像。最近受到关注的是能够利用荧光特性(而非强度)的技术发展,例如荧光团的发射光谱和激发态寿命。光谱可用于区分荧光团,寿命可用于报告荧光团的微环境。我们描述了一种新颖的技术——联合光谱和寿命成像,它结合了多光子显微镜、光谱鉴别和寿命分析的优点,并允许同时收集所有三个维度的数据以及空间和时间信息。