AbstractTryptophan is widely used as an intrinsic fluorophore for studies of protein structure and dynamics. Its fluorescence is known to have two decay components with lifetimes of 0.5 and 3.1 ns. In this work we measure the ultrafast dynamics of Tryptophan at <100 fs through measurements and modeling of the Raman excitation profiles with time-dependent wave packet propagation theory. We use a Brownian oscillator model to simulate the water-tryptophan interaction. Upon photoexcitation to the higher singlet electronic state (Bb) the structure of tryptophan is distorted to an overall expansion of the pyrrole and benzene rings. The total reorganization energy for Trp in water is estimated to be 2169 cm−1 with a 1230 cm−1 contribution from the...
We report here studies of tryptophan (Trp) solvation dynamics in water and in the Pyrococcus furiosu...
AbstractTryptophan fluorescence wavelength is widely used as a tool to monitor changes in proteins a...
AbstractThe dynamics of single tryptophan (W) side chain of protease subtilisin Carlsberg (SC) and m...
AbstractTryptophan is widely used as an intrinsic fluorophore for studies of protein structure and d...
: By combining UV transient absorption spectroscopy with sub-30-fs temporal resolution and CASPT2/MM...
To better understand the complex photophysics of the amino acid tryptophan, which is widely used as ...
The study of the photodetachment of amino acids in aqueous solution is pertinent to the understandin...
Tryptophan is one of the three natural aromatic amino acids and can serve as local probe of photorea...
AbstractWe compare UV transient grating (TG) experiments of aqueous tryptophan with transient absorp...
The interactions of tryptophan-59 (TRP-59) and its protein environment in ribonuclease-T1 (RNAse-T1)...
Author Institution: Department of Physics, The Ohio State University, Columbus, Oh, 43210Although tr...
The first objective of our research was to accurately measure the phosphorescence lifetime of aqueou...
Time dependent fluorescence Stokes (emission wavelength) shifts (TDFSS) from tryptophan (Trp) follow...
ii Proteins are dynamical in nature. Their ability to function relies on their overall flexibility. ...
The single room temperature phosphorescent (RTP) residue of horse liver alcohol dehydrogenase (LADH)...
We report here studies of tryptophan (Trp) solvation dynamics in water and in the Pyrococcus furiosu...
AbstractTryptophan fluorescence wavelength is widely used as a tool to monitor changes in proteins a...
AbstractThe dynamics of single tryptophan (W) side chain of protease subtilisin Carlsberg (SC) and m...
AbstractTryptophan is widely used as an intrinsic fluorophore for studies of protein structure and d...
: By combining UV transient absorption spectroscopy with sub-30-fs temporal resolution and CASPT2/MM...
To better understand the complex photophysics of the amino acid tryptophan, which is widely used as ...
The study of the photodetachment of amino acids in aqueous solution is pertinent to the understandin...
Tryptophan is one of the three natural aromatic amino acids and can serve as local probe of photorea...
AbstractWe compare UV transient grating (TG) experiments of aqueous tryptophan with transient absorp...
The interactions of tryptophan-59 (TRP-59) and its protein environment in ribonuclease-T1 (RNAse-T1)...
Author Institution: Department of Physics, The Ohio State University, Columbus, Oh, 43210Although tr...
The first objective of our research was to accurately measure the phosphorescence lifetime of aqueou...
Time dependent fluorescence Stokes (emission wavelength) shifts (TDFSS) from tryptophan (Trp) follow...
ii Proteins are dynamical in nature. Their ability to function relies on their overall flexibility. ...
The single room temperature phosphorescent (RTP) residue of horse liver alcohol dehydrogenase (LADH)...
We report here studies of tryptophan (Trp) solvation dynamics in water and in the Pyrococcus furiosu...
AbstractTryptophan fluorescence wavelength is widely used as a tool to monitor changes in proteins a...
AbstractThe dynamics of single tryptophan (W) side chain of protease subtilisin Carlsberg (SC) and m...