红外光谱学
光谱学
水溶液
化学
红外线的
蛋白质二级结构
结晶学
折叠(DSP实现)
和频发生光谱学
化学物理
分析化学(期刊)
物理化学
和频产生
有机化学
光学
物理
工程类
电气工程
非线性光学
激光器
量子力学
生物化学
作者
Adam S. Chatterley,Thaddeus W. Golbek,Tobias Weidner
标识
DOI:10.1021/acs.jpclett.2c01324
摘要
Determining the secondary and tertiary structures of proteins at aqueous interfaces is crucial for understanding their function, but measuring these structures selectively at the interface is challenging. Here we demonstrate that two-dimensional infrared (2D-IR) spectroscopy of protein stabilized emulsions offers a new route to measuring interfacial protein structure with high levels of detail. We prepared hexadecane/water oil-in-water emulsions stabilized by model LK peptides that are known to fold into either α-helix or β-sheet conformations at hydrophobic interfaces and measured 2D-IR spectra in a transmission geometry. We saw clear spectral signatures of the peptides folding at the interface, with no detectable residue from remaining bulk peptides. Using 2D spectroscopy gives us access to correlation and dynamics data, which enables structural assignment in cases where linear spectroscopy fails. Using the emulsions allows one to study interfacial spectra with standard transmission geometry spectrometers, bringing the richness of 2D-IR to the interface with no additional optical complexity.
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