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首页> 外文期刊>Analytical chemistry >The Next Generation of IR Spectroscopy: EC-QCL-Based Mid-IR Transmission Spectroscopy of Proteins with Balanced Detection
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The Next Generation of IR Spectroscopy: EC-QCL-Based Mid-IR Transmission Spectroscopy of Proteins with Balanced Detection

机译:下一代IR光谱:基于EC-QCL的MID-IR透射光谱,具有平衡检测

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We report a mid-IR transmission setup for the analysis of the protein amide I and amide II band in aqueous solutions that achieves a limit of detection as low as 0.0025 mg mL(-)(1) (outperforming our previous results and other state-of-the-art mid-IR-based techniques by almost an order of magnitude). This large improvement is made possible by combining the latest-generation external cavity-quantum cascade laser (EC-QCL) operated at room temperature with an optimized double-beam optical setup that adjusts the path length (26 mu m) to ensure robust sample handling. For minimizing the noise introduced by the high-intensity laser light source, a thermoelectrically cooled mercury cadmium telluride balanced detection module was employed. In this way, noise levels better by a factor of up to 20 were achieved compared with single-channel measurements. Characteristic spectral features of proteins with different secondary structures were successfully identified at concentrations as low as 0.1 mg mL(-1). Furthermore, a highly linear response was demonstrated for concentrations between 0.05 and 10 mg mL(-1). The total acquisition time of the setup can be adapted to fulfill the required sensitivity of the protein measurements and to ensure maximum flexibility for future applications. The presented setup combines high sensitivity, large optical path lengths, and short measurement times and thus outperforms previous research type EC-QCL setups as well as commercially available instruments. This opens a wide range of future applications including protein-ligand interaction studies as well as qualitative and quantitative analyses of proteins in complex matrices such as those found in up- and downstream bioprocess monitoring and similar challenging applications which can not be readily met by conventional FT-IR spectroscopy.
机译:我们在水溶液中报告了用于分析蛋白酰胺I和酰胺II带的中红外变速器设置,该水溶液中的检测限为低至0.0025mg ml( - )(1)(优于我们以前的结果和其他国家 - 最重要的中间IR基技巧几乎是一个数量级)。通过将在室温下操作的最新一代外腔 - 量子级联激光器(EC-QCL)与优化的双梁光学设置相结合,可以通过优化的双梁光学设置来实现这一大改进,可调整路径长度(26 mu m)以确保鲁棒样品处理。为了使高强度激光光源引入的噪声最小化,采用了热电冷却汞镉碲化镉平衡检测模块。以这种方式,与单通道测量相比,达到了多达20个倍数最多的噪声水平。以低至0.1mg ml(-1)的浓度成功鉴定具有不同二次结构的蛋白质的特征谱特征。此外,对0.05-10mg ml(-1)之间的浓度证明了高线性响应。设置的总采集时间可以适用于满足蛋白质测量的所需灵敏度,并确保未来应用的最大灵活性。所提出的设置结合了高灵敏度,大光路长度和短测量时间,从而优于先前的研究类型EC-QCL设置以及市售的仪器。这开辟了广泛的未来应用,包括蛋白质 - 配体相互作用研究,以及复杂矩阵中的蛋白质的定性和定量分析,例如在上游生物过程监测和类似具有挑战性的应用中,不能通过常规FT容易地满足-ir光谱。

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