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External cavity-quantum cascade laser infrared spectroscopy for secondary structure analysis of proteins at low concentrations

机译:外腔 - 量子级联激光红外光谱,用于低浓度蛋白质的二次结构分析

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摘要

Fourier transform infrared (FTIR) and circular dichroism (CD) spectroscopy are analytical techniques employed for the analysis of protein secondary structure. The use of CD spectroscopy is limited to low protein concentrations (5?mg ml(-1)). Here we introduce a quantum cascade laser (QCL)-based IR transmission setup for analysis of protein and polypeptide secondary structure at concentrations as low as 0.25?mg ml(-1) in deuterated buffer solution. We present dynamic QCL-IR spectra of the temperature-induced α-helix to β-sheet transition of poly-L-lysine. The concentration dependence of the α-β transition temperature between 0.25 and 10?mg ml(-1) was investigated by QCL-IR, FTIR and CD spectroscopy. By using QCL-IR spectroscopy it is possible to perform IR spectroscopic analysis in the same concentration range as CD spectroscopy, thus enabling a combined analysis of biomolecules secondary structure by CD and IR spectroscopy.
机译:傅里叶变换红外(FTIR)和圆形二色性(CD)光谱是用于分析蛋白质二级结构的分析技术。使用CD光谱仅限于低蛋白质浓度(5×Mg ml(-1))。在这里,我们介绍了用于在氘代缓冲溶液中以低至0.25×mg ml(-1)的浓度为低至0.25×mg(-1)的蛋白质和多肽二级结构的量子级联激光(QCl)。我们呈现温度诱导的α-螺旋的动态QCL-IR光谱到聚-L-赖氨酸的β-薄膜过渡。通过QCl-IR,FTIR和CD光谱研究了α-β转变温度的α-β转变温度的浓度依赖性依赖于0.25和10×mg ml(-1)。通过使用QCL-IR光谱,可以在与CD光谱相同的浓度范围内进行IR光谱分析,从而通过CD和IR光谱能够组合生物分子二次结构的分析。

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