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Chiral Vibrational Structures of Proteins at Interfaces Probed by Sum Frequency Generation Spectroscopy

机译:求和频率产生光谱探测界面上蛋白质的手性振动结构。

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摘要

We review the recent development of chiral sum frequency generation (SFG) spectroscopy and its applications to study chiral vibrational structures at interfaces. This review summarizes observations of chiral SFG signals from various molecular systems and describes the molecular origins of chiral SFG response. It focuses on the chiral vibrational structures of proteins and presents the chiral SFG spectra of proteins at interfaces in the C-H stretch, amide I, and N-H stretch regions. In particular, a combination of chiral amide I and N-H stretches of the peptide backbone provides highly characteristic vibrational signatures, unique to various secondary structures, which demonstrate the capacity of chiral SFG spectroscopy to distinguish protein secondary structures at interfaces. On the basis of these recent developments, we further discuss the advantages of chiral SFG spectroscopy and its potential application in various fields of science and technology. We conclude that chiral SFG spectroscopy can be a new approach to probe chiral vibrational structures of protein at interfaces, providing structural and dynamic information to study in situ and in real time protein structures and dynamics at interfaces.
机译:我们审查了手性和频率生成(SFG)光谱学的最新发展及其在研究界面上的手性振动结构的应用。这篇综述总结了来自各种分子系统的手性SFG信号的观察结果,并描述了手性SFG反应的分子起源。它着重于蛋白质的手性振动结构,并提供了C-H伸展,酰胺I和N-H伸展区域的界面上蛋白质的手性SFG光谱。特别地,手性酰胺I和肽骨架的N-H片段的组合提供了各种二级结构所独有的高度特征性的振动特征,这表明手性SFG光谱学能够区分界面处的蛋白二级结构。在这些最新进展的基础上,我们进一步讨论了手性SFG光谱的优势及其在各个科学技术领域的潜在应用。我们得出的结论是,手性SFG光谱学可以成为一种探查界面上蛋白质的手性振动结构的新方法,提供结构和动态信息,以就地和实时研究界面处的蛋白质结构和动力学。

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