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Femtosecond Stimulated Raman Study of Excited-state Evolution in Bacteriorhodopsin

Overview
Journal J Phys Chem B
Specialty Chemistry
Date 2006 Jul 21
PMID 16852266
Citations 18
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Abstract

Femtosecond time-resolved stimulated Raman spectroscopy (FSRS) is used to examine the photoisomerization dynamics in the excited state of bacteriorhodopsin. Near-IR stimulated emission is observed in the FSRS probe window that decays with a 400-600-fs time constant. Additionally, dispersive vibrational lines appear at the locations of the ground-state vibrational frequencies and decay with a 260-fs time constant. The dispersive line shapes are caused by a nonlinear effect we term Raman initiated by nonlinear emission (RINE) that generates vibrational coherence on the ground-state surface. Theoretical expressions for the RINE line shapes are developed and used to fit the spectral and temporal evolution of the spectra. The rapid 260-fs decay of the RINE peak intensity, compared to the slower evolution of the stimulated emission, indicates that the excited-state population moves in approximately 260 fs to a region on the potential energy surface where the RINE signal is attenuated. This loss of RINE signal is best explained by structural evolution of the excited-state population along multiple low-frequency modes that carry the molecule out of the harmonic photochemically inactive Franck-Condon region and into the photochemically active geometry.

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References
1.
Herbst J, Heyne K, Diller R . Femtosecond infrared spectroscopy of bacteriorhodopsin chromophore isomerization. Science. 2002; 297(5582):822-5. DOI: 10.1126/science.1072144. View

2.
Lee S, Zhang D, McCamant D, Kukura P, Mathies R . Theory of femtosecond stimulated Raman spectroscopy. J Chem Phys. 2004; 121(8):3632-42. PMC: 1752224. DOI: 10.1063/1.1777214. View

3.
Braiman M, Mathies R . Resonance Raman evidence for an all-trans to 13-cis isomerization in the proton-pumping cycle of bacteriorhodopsin. Biochemistry. 1980; 19(23):5421-8. DOI: 10.1021/bi00564a042. View

4.
Gai F, Hasson K, McDonald J, Anfinrud P . Chemical dynamics in proteins: the photoisomerization of retinal in bacteriorhodopsin. Science. 1998; 279(5358):1886-91. DOI: 10.1126/science.279.5358.1886. View

5.
Lanyi J . Understanding structure and function in the light-driven proton pump bacteriorhodopsin. J Struct Biol. 1999; 124(2-3):164-78. DOI: 10.1006/jsbi.1998.4044. View