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用于低浓度蛋白质快速灵敏分析的外腔量子级联激光振动圆二色光谱法

External Cavity Quantum Cascade Laser Vibrational Circular Dichroism Spectroscopy for Fast and Sensitive Analysis of Proteins at Low Concentrations.

作者信息

Hermann Daniel-Ralph, Ramer Georg, Lendl Bernhard

出版信息

Anal Chem. 2024 Dec 10;96(49):19363-19369. doi: 10.1021/acs.analchem.4c03498. Epub 2024 Nov 22.

Abstract

Proteins are characterized by their complex levels of structures, which in turn define their function. Understanding and evaluating these structures is therefore crucial to illuminating biological processes. One of the possible analytical methods is vibrational circular dichroism (VCD), which expands the structural sensitivity of classical infrared (IR) absorbance spectroscopy by the chiral sensitivity of circular dichroism. While this technique is powerful, it is plagued by low signal intensities and long measurement times. Here we present an optical setup leveraging the high brilliance of a quantum cascade laser to measure proteins in DO at a path length of 204 μm. It was compared to classical Fourier-transform infrared spectroscopy (FT-IR) in terms of noise levels and in its applicability to secondary structure elucidation of proteins. Protein concentrations as low as 2 mg/mL were accessible by the laser-based system at a measurement time of 1 h. Further increase of the time resolution was possible by adapting the emission to cover only the amide I' band. This allowed for the collection of spectral data at a measurement time of 5 min without a loss of performance. With this high time resolution, we are confident that dynamic processes of protein can now be monitored by VCD, increasing our understanding of these reactions.

摘要

蛋白质具有复杂的结构层次,这些结构层次反过来又决定了它们的功能。因此,理解和评估这些结构对于阐明生物过程至关重要。一种可能的分析方法是振动圆二色性(VCD),它通过圆二色性的手性敏感性扩展了经典红外(IR)吸收光谱的结构敏感性。虽然这项技术很强大,但它受到低信号强度和长测量时间的困扰。在这里,我们展示了一种光学装置,利用量子级联激光器的高亮度,在204μm的光程长度下测量溶解在重水中的蛋白质。我们将其与经典傅里叶变换红外光谱(FT-IR)在噪声水平及其对蛋白质二级结构解析的适用性方面进行了比较。基于激光的系统在1小时的测量时间内可以检测到低至2mg/mL的蛋白质浓度。通过调整发射使其仅覆盖酰胺I'带,可以进一步提高时间分辨率。这使得在5分钟的测量时间内收集光谱数据而不损失性能成为可能。有了这种高时间分辨率,我们相信现在可以通过VCD监测蛋白质的动态过程,加深我们对这些反应的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b26/11635754/136762f6f207/ac4c03498_0001.jpg

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