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Ultrafast pH-jump two-dimensional infrared spectroscopy
Author(s) -
Jennifer C. Flanagan,
Carlos R. Baiz
Publication year - 2019
Publication title -
optics letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.524
H-Index - 272
eISSN - 1071-2763
pISSN - 0146-9592
DOI - 10.1364/ol.44.004937
Subject(s) - femtosecond , nanosecond , protonation , ultrashort pulse , dissociation (chemistry) , spectroscopy , two dimensional infrared spectroscopy , infrared , infrared spectroscopy , materials science , chemistry , analytical chemistry (journal) , photochemistry , optics , laser , physics , ion , organic chemistry , chromatography , quantum mechanics
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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