Interplays of electron and nuclear motions along CO dissociation trajectory in myoglobin revealed by ultrafast X-rays and quantum dynamics calculations.
X-ray transient absorption
myoglobin
protein structural dynamics
quantum dynamics calculation
time-resolved solution X-ray scattering
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
06 04 2021
06 04 2021
Historique:
entrez:
30
3
2021
pubmed:
31
3
2021
medline:
20
11
2021
Statut:
ppublish
Résumé
Ultrafast structural dynamics with different spatial and temporal scales were investigated during photodissociation of carbon monoxide (CO) from iron(II)-heme in bovine myoglobin during the first 3 ps following laser excitation. We used simultaneous X-ray transient absorption (XTA) spectroscopy and X-ray transient solution scattering (XSS) at an X-ray free electron laser source with a time resolution of 80 fs. Kinetic traces at different characteristic X-ray energies were collected to give a global picture of the multistep pathway in the photodissociation of CO from heme. In order to extract the reaction coordinates along different directions of the CO departure, XTA data were collected with parallel and perpendicular relative polarizations of the laser pump and X-ray probe pulse to isolate the contributions of electronic spin state transition, bond breaking, and heme macrocycle nuclear relaxation. The time evolution of the iron K-edge X-ray absorption near edge structure (XANES) features along the two major photochemical reaction coordinates, i.e., the iron(II)-CO bond elongation and the heme macrocycle doming relaxation were modeled by time-dependent density functional theory calculations. Combined results from the experiments and computations reveal insight into interplays between the nuclear and electronic structural dynamics along the CO photodissociation trajectory. Time-resolved small-angle X-ray scattering data during the same process are also simultaneously collected, which show that the local CO dissociation causes a protein quake propagating on different spatial and temporal scales. These studies are important for understanding gas transport and protein deligation processes and shed light on the interplay of active site conformational changes and large-scale protein reorganization.
Identifiants
pubmed: 33782122
pii: 2018966118
doi: 10.1073/pnas.2018966118
pmc: PMC8040624
pii:
doi:
Substances chimiques
Myoglobin
0
Heme
42VZT0U6YR
Carbon Monoxide
7U1EE4V452
Iron
E1UOL152H7
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIGMS NIH HHS
ID : P41 GM118217
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM115761
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008382
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL063203
Pays : United States
Déclaration de conflit d'intérêts
The authors declare no competing interest.
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