Fischer Martin C, Wilson Jesse W, Robles Francisco E, Warren Warren S
Department of Chemistry, Duke University, Durham, North Carolina 27708, USA.
Departments of Chemistry, Biomedical Engineering, Physics, and Radiology, Duke University, Durham, North Carolina 27708, USA.
Rev Sci Instrum. 2016 Mar;87(3):031101. doi: 10.1063/1.4943211.
Multiphoton microscopy has rapidly gained popularity in biomedical imaging and materials science because of its ability to provide three-dimensional images at high spatial and temporal resolution even in optically scattering environments. Currently the majority of commercial and home-built devices are based on two-photon fluorescence and harmonic generation contrast. These two contrast mechanisms are relatively easy to measure but can access only a limited range of endogenous targets. Recent developments in fast laser pulse generation, pulse shaping, and detection technology have made accessible a wide range of optical contrasts that utilize multiple pulses of different colors. Molecular excitation with multiple pulses offers a large number of adjustable parameters. For example, in two-pulse pump-probe microscopy, one can vary the wavelength of each excitation pulse, the detection wavelength, the timing between the excitation pulses, and the detection gating window after excitation. Such a large parameter space can provide much greater molecular specificity than existing single-color techniques and allow for structural and functional imaging without the need for exogenous dyes and labels, which might interfere with the system under study. In this review, we provide a tutorial overview, covering principles of pump-probe microscopy and experimental setup, challenges associated with signal detection and data processing, and an overview of applications.
多光子显微镜在生物医学成像和材料科学领域迅速受到欢迎,因为即使在光学散射环境中,它也能够以高空间和时间分辨率提供三维图像。目前,大多数商业和自制设备都基于双光子荧光和谐波产生对比度。这两种对比度机制相对容易测量,但只能检测有限范围内的内源性目标。快速激光脉冲产生、脉冲整形和检测技术的最新进展使得利用多种不同颜色脉冲的广泛光学对比度成为可能。多脉冲分子激发提供了大量可调节参数。例如,在双脉冲泵浦-探测显微镜中,可以改变每个激发脉冲的波长、检测波长、激发脉冲之间的时间以及激发后的检测选通窗口。如此大的参数空间可以提供比现有单色技术更高的分子特异性,并允许在无需外源性染料和标记的情况下进行结构和功能成像,因为这些染料和标记可能会干扰正在研究的系统。在本综述中,我们提供了一个教程概述,涵盖泵浦-探测显微镜的原理和实验设置、与信号检测和数据处理相关的挑战以及应用概述。