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The effect of optical substrates on micro-FTIR analysis of single mammalian cells

机译:光学基质对单个哺乳动物细胞的显微FTIR分析的影响

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The study of individual cells with infrared (IR) microspectroscopy often requires living cells to be cultured directly onto a suitable substrate. The surface effect of the specific substrates on the cell growth—viability and associated biochemistry—as well as on the IR analysis—spectral interference and optical artifacts—is all too often ignored. Using the IR beamline, MIRIAM (Diamond Light Source, UK), we show the importance of the substrate used for IR absorption spectroscopy by analyzing two different cell lines cultured on a range of seven optical substrates in both transmission and reflection modes. First, cell viability measurements are made to determine the preferable substrates for normal cell growth. Successively, synchrotron radiation IR microspectroscopy is performed on the two cell lines to determine any genuine biochemically induced changes or optical effect in the spectra due to the different substrates. Multivariate analysis of spectral data is applied on each cell line to visualize the spectral changes. The results confirm the advantage of transmission measurements over reflection due to the absence of a strong optical standing wave artifact which amplifies the absorbance spectrum in the high wavenumber regions with respect to low wavenumbers in the mid-IR range. The transmission spectra reveal interference from a more subtle but significant optical artifact related to the reflection losses of the different substrate materials. This means that, for comparative studies of cell biochemistry by IR microspectroscopy, it is crucial that all samples are measured on the same substrate type.
机译:用红外(IR)光谱学研究单个细胞通常需要将活细胞直接培养在合适的基质上。通常会忽略特定底物对细胞生长(活力和相关的生物化学)以及对IR分析(光谱干扰和光学伪影)的表面影响。通过使用红外光束线MIRIAM(英国钻石光源,英国),我们通过分析在透射和反射模式下在七个光学基板范围内培养的两种不同细胞系,显示了用于红外吸收光谱的基板的重要性。首先,进行细胞活力测定以确定正常细胞生长的优选底物。随后,对这两个细胞系进行同步辐射红外光谱分析,以确定由于不同底物而引起的任何真正的生化诱导变化或光谱中的光学效应。将光谱数据的多变量分析应用于每个细胞系以可视化光谱变化。该结果证实了透射测量相对于反射的优势,这是因为不存在强的光学驻波伪像,该伪像不会对中红外范围内的低波数放大高波数区域中的吸收光谱。透射光谱揭示出来自与不同基板材料的反射损耗有关的更微妙但重要的光学伪影的干扰。这意味着,对于通过IR显微光谱进行细胞生物化学的比较研究,至关重要的是,所有样品都必须在相同的底物类型上进行测量。

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