纳秒
飞秒
质子化
离解(化学)
超短脉冲
光谱学
红外光谱学
红外线的
二维红外光谱
材料科学
化学
光化学
分析化学(期刊)
光学
物理化学
激光器
物理
离子
有机化学
量子力学
色谱法
作者
Jennifer C. Flanagan,Carlos R. Baiz
出处
期刊:Optics Letters
[The Optical Society]
日期:2019-10-15
卷期号:44 (20): 4937-4937
被引量:4
摘要
We present a pH-jump two-dimensional infrared (2D IR) spectrometer to probe pH-dependent conformational changes from nanoseconds to milliseconds. The design incorporates a nanosecond 355 nm source into a pulse-shaper-based 2D IR spectrometer to trigger dissociation of a caged proton prior to probing subsequent conformational changes with femtosecond 2D IR spectroscopy. We observe a blue shift in the amide I mode (C═O stretch) of diglycine induced by protonation of the terminal amine. This method combines the bond-specific structural sensitivity of ultrafast 2D IR with triggered conformational dynamics, providing structural access to multiscale biomolecular transformations such as protein folding.
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