首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Differential Imaging of Biological Structures with Doubly-resonant Coherent Anti-stokes Raman Scattering (CARS)
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Differential Imaging of Biological Structures with Doubly-resonant Coherent Anti-stokes Raman Scattering (CARS)

机译:双共振相干反斯托克斯拉曼散射(CARS)的生物结构的差分成像。

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摘要

Coherent Raman imaging techniques have seen a dramatic increase in activity over the past decade due to their promise to enable label-free optical imaging with high molecular specificity 1. The sensitivity of these techniques, however, is many orders of magnitude weaker than fluorescence, requiring milli-molar molecular concentrations 1,2. Here, we describe a technique that can enable the detection of weak or low concentrations of Raman-active molecules by amplifying their signal with that obtained from strong or abundant Raman scatterers. The interaction of short pulsed lasers in a biological sample generates a variety of coherent Raman scattering signals, each of which carry unique chemical information about the sample. Typically, only one of these signals, e.g. Coherent Anti-stokes Raman scattering (CARS), is used to generate an image while the others are discarded. However, when these other signals, including 3-color CARS and four-wave mixing (FWM), are collected and compared to the CARS signal, otherwise difficult to detect information can be extracted 3. For example, doubly-resonant CARS (DR-CARS) is the result of the constructive interference between two resonant signals 4. We demonstrate how tuning of the three lasers required to produce DR-CARS signals to the 2845 cm-1 CH stretch vibration in lipids and the 2120 cm-1 CD stretching vibration of a deuterated molecule (e.g. deuterated sugars, fatty acids, etc.) can be utilized to probe both Raman resonances simultaneously. Under these conditions, in addition to CARS signals from each resonance, a combined DR-CARS signal probing both is also generated. We demonstrate how detecting the difference between the DR-CARS signal and the amplifying signal from an abundant molecule's vibration can be used to enhance the sensitivity for the weaker signal. We further demonstrate that this approach even extends to applications where both signals are generated from different molecules, such that e.g. using the strong Raman signal of a solvent can enhance the weak Raman signal of a dilute solute.
机译:过去十年来,相干拉曼成像技术的活性有了显着提高,这是因为它们有望实现具有高分子特异性 1 的无标记光学成像。但是,这些技术的灵敏度比荧光弱很多数量级,因此需要分子摩尔浓度 1,2 。在这里,我们描述了一种技术,该技术可以通过使用从强拉曼散射体或丰富拉曼散射体获得的信号放大信号来检测弱浓度或低浓度的拉曼活性分子。生物样品中短脉冲激光的相互作用会产生各种相干拉曼散射信号,每个信号都携带有关样品的独特化学信息。通常,这些信号中只有一个,例如相干反斯托克斯拉曼散射(CARS)用于生成图像,而其他图像则被丢弃。但是,当收集这些其他信号(包括三色CARS和四波混频(FWM))并将其与CARS信号进行比较时,可以提取 3 来提取难以检测的信息。例如,双共振CARS(DR-CARS)是两个共振信号 4 之间的相长干涉的结果。我们演示了如何调整产生DR-CARS信号所需的三个激光,使其在脂质中的2845 cm -1 CH拉伸振动和在2120 cm -1 CD的拉伸振动中调谐。氘代分子(例如,氘代糖,脂肪酸等)可用于同时探测两个拉曼共振。在这些条件下,除了来自每个共振的CARS信号之外,还生成了探测两者的组合DR-CARS信号。我们演示了如何检测DR-CARS信号与来自丰富分子振动的放大信号之间的差异,可以用来增强对较弱信号的灵敏度。我们进一步证明,该方法甚至扩展到两种信号均由不同分子产生的应用,例如使用溶剂的强拉曼信号可以增强稀释溶质的弱拉曼信号。

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