Weeks Tyler J, Huser Thomas R
Center for Biophotonics, University of California, Davis, USA.
J Vis Exp. 2010 Oct 17(44):2085. doi: 10.3791/2085.
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. The sensitivity of these techniques, however, is many orders of magnitude weaker than fluorescence, requiring milli-molar molecular concentrations. 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. For example, doubly-resonant CARS (DR-CARS) is the result of the constructive interference between two resonant signals. 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.
在过去十年中,相干拉曼成像技术的应用急剧增加,因为它们有望实现具有高分子特异性的无标记光学成像。然而,这些技术的灵敏度比荧光弱许多个数量级,需要毫摩尔级的分子浓度。在此,我们描述了一种技术,该技术可以通过用强或丰富的拉曼散射体获得的信号来放大弱或低浓度拉曼活性分子的信号,从而实现对其的检测。短脉冲激光在生物样品中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,而其他信号则被丢弃。然而,当收集这些其他信号,包括三色CARS和四波混频(FWM),并与CARS信号进行比较时,可以提取出原本难以检测到的信息。例如,双共振CARS(DR-CARS)是两个共振信号之间相长干涉的结果。我们展示了如何将产生DR-CARS信号所需的三个激光调谐到脂质中2845 cm⁻¹的CH伸缩振动以及氘代分子(如氘代糖、脂肪酸等)的2120 cm⁻¹ CD伸缩振动,以便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信号外,还会产生一个同时探测两者的组合DR-CARS信号。我们展示了如何检测DR-CARS信号与丰富分子振动的放大信号之间的差异,以增强对较弱信号的灵敏度。我们进一步证明,这种方法甚至扩展到两个信号由不同分子产生的应用中,例如使用溶剂的强拉曼信号可以增强稀溶液溶质的弱拉曼信号。