School of Biomedical Engineering, Department of Electrical and Computer Engineering, and Department of Chemistry, Colorado State University, Fort Collins, CO 80521.
Proc Natl Acad Sci U S A. 2013 Nov 12;110(46):18391-6. doi: 10.1073/pnas.1306856110. Epub 2013 Oct 30.
Optical microscopy has played a critical role for discovery in biomedical sciences since Hooke's introduction of the compound microscope. Recent years have witnessed explosive growth in optical microscopy tools and techniques. Information in microscopy is garnered through contrast mechanisms, usually absorption, scattering, or phase shifts introduced by spatial structure in the sample. The emergence of nonlinear optical contrast mechanisms reveals new information from biological specimens. However, the intensity dependence of nonlinear interactions leads to weak signals, preventing the observation of high-speed dynamics in the 3D context of biological samples. Here, we show that for second harmonic generation imaging, we can increase the 3D volume imaging speed from sub-Hertz speeds to rates in excess of 1,500 volumes imaged per second. This transformational capability is possible by exploiting coherent scattering of second harmonic light from an entire specimen volume, enabling new observational capabilities in biological systems.
光学显微镜自 Hooke 引入复合显微镜以来,在生物医学科学的发现中发挥了关键作用。近年来,光学显微镜工具和技术呈爆炸式增长。显微镜中的信息是通过对比度机制获得的,通常是通过样品中的空间结构引入的吸收、散射或相移。非线性光学对比度机制的出现揭示了生物标本的新信息。然而,非线性相互作用的强度依赖性导致信号较弱,阻止了在生物样本的 3D 环境中观察高速动力学。在这里,我们表明,对于二次谐波产生成像,我们可以将 3D 体积成像速度从亚赫兹速度提高到每秒超过 1500 个体积成像的速度。通过利用二次谐波光从整个样品体积的相干散射,这种变革性的能力成为可能,从而在生物系统中实现新的观测能力。