Time-resolved infrared spectroscopy with 0.5-ps resolution is used to track the evolution of the CO stretching vibration after visible photoexcitation of carboxyhemoglobin in water at room temperature. Polarization measurements determine that the iron-complexed CO is oriented nearly perpendicular to the porphyrin plane. The dissociation appears to proceed via a metastable excited state with 2 +/- 1 ps lifetime. The dissociated CO binds weakly in the heme pocket for at least 500 ps. This state correlates with the internally bound state observed by Frauenfelder et al. at low temperatures in myoglobin
International audienceWe report spectrally-integrated, visible-pump, mid-infrared probe studies of t...
Molecular dynamics simulations of the photodissociated state of carbonmonoxy myoglobin (MbCO) are pr...
The FixL proteins are heme-based bacterial oxygen sensors, distinct from globins in structure and li...
Time-resolved infrared spectroscopy with 0.5-ps resolution is used to track the evolution of the CO ...
International audienceWe used a femtosecond visible-infrared pump-probe experiment to follow ligand ...
International audienceWe investigate ultrafast vibrational ligand dynamics in carboxyhemoglobin usin...
Author Institution: Department of Chemistry, Harvard UniversityLigand association to and dissociatio...
Infrared spectra of carbon monoxide bound myoglobin reveal several lines due only to the carbon mono...
International audienceWe report femtosecond visible pump, midinfrared probe, spectrally integrated e...
Carbon monoxide recombination dynamics upon photodissociation with visible light has been characteri...
AbstractMolecular dynamics simulations of the photodissociated state of carbonmonoxy myoglobin (MbCO...
We have studied ultrafast dynamics in two systems: heme proteins and small de novo peptides. Heme re...
International audienceUltrafast structural dynamics with different spatial and temporal scales were ...
Cytochrome P450BM3 is a bacterial enzyme with a heme cofactor that binds small diatomic ligands. Her...
This thesis deals with applications of femtosecond infrared (IR) spectroscopy to chemical and biolog...
International audienceWe report spectrally-integrated, visible-pump, mid-infrared probe studies of t...
Molecular dynamics simulations of the photodissociated state of carbonmonoxy myoglobin (MbCO) are pr...
The FixL proteins are heme-based bacterial oxygen sensors, distinct from globins in structure and li...
Time-resolved infrared spectroscopy with 0.5-ps resolution is used to track the evolution of the CO ...
International audienceWe used a femtosecond visible-infrared pump-probe experiment to follow ligand ...
International audienceWe investigate ultrafast vibrational ligand dynamics in carboxyhemoglobin usin...
Author Institution: Department of Chemistry, Harvard UniversityLigand association to and dissociatio...
Infrared spectra of carbon monoxide bound myoglobin reveal several lines due only to the carbon mono...
International audienceWe report femtosecond visible pump, midinfrared probe, spectrally integrated e...
Carbon monoxide recombination dynamics upon photodissociation with visible light has been characteri...
AbstractMolecular dynamics simulations of the photodissociated state of carbonmonoxy myoglobin (MbCO...
We have studied ultrafast dynamics in two systems: heme proteins and small de novo peptides. Heme re...
International audienceUltrafast structural dynamics with different spatial and temporal scales were ...
Cytochrome P450BM3 is a bacterial enzyme with a heme cofactor that binds small diatomic ligands. Her...
This thesis deals with applications of femtosecond infrared (IR) spectroscopy to chemical and biolog...
International audienceWe report spectrally-integrated, visible-pump, mid-infrared probe studies of t...
Molecular dynamics simulations of the photodissociated state of carbonmonoxy myoglobin (MbCO) are pr...
The FixL proteins are heme-based bacterial oxygen sensors, distinct from globins in structure and li...