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Time-Resolved Spectroscopy of Ultrafast Photoisomerization of Octopus Rhodopsin under Photoexcitation
Author(s) -
Atsushi Yabushita,
Takayoshi Kobayashi,
Motoyuki Tsuda
Publication year - 2012
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/jp209356s
Subject(s) - photoexcitation , rhodopsin , photoisomerization , conical intersection , bacteriorhodopsin , spectroscopy , resonance raman spectroscopy , chemistry , chromophore , ultrashort pulse , materials science , molecular physics , photochemistry , retinal , atomic physics , raman spectroscopy , physics , laser , optics , excited state , isomerization , biochemistry , quantum mechanics , membrane , catalysis
A primary process in vision is the cis-trans photoisomerization of a chromophore of rhodopsin, called retinal. In the present work, we have performed ultrafast time-resolved spectroscopy of octopus rhodopsin using a sub-5-fs pulse laser. In comparison with our previous study on bacteriorhodopsin, we found that octopus rhodopsin follows similar dynamics after photoexcitation but with different time constants. Spectrogram analysis showed that a C═N stretching mode appeared directly after photoexcitation. After reaching the conical intersection region at 80 fs, the overlapping hydrogen out-of-plane and in-plane C═C-H modes emerged as distinct peaks at ~200 fs, finishing a rapid relaxation along the coordinate related with these modes. The intensities of these peaks and a C═C stretching mode were found to be modulated at a period of ∼500 fs, reflecting torsional motion around the C═C double bond before thermalization with the distribution of structural variations in the all-trans structure in configuration space.

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