Back to Search
Start Over
Ultrafast X-ray Spectroscopy of Haem Proteins
- Source :
- CHIMIA. 76:538
- Publication Year :
- 2022
- Publisher :
- Swiss Chemical Society, 2022.
-
Abstract
- In this article we revisit our recent picosecond and femtosecond X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES) experiments, probing the ultrafast electronic and geometric evolution of photoexcited haem proteins, namely ferrous Nitrosyl Myoglobin (MbNO) and ferric Cytochrome c (Cyt c). We show through these two examples, combined with results from ultrafast optical spectroscopy, the universal behavior of the excited state dynamics of ferric and ferrous complexes. Regardless of the type of ligand, its dissociation or lack thereof, or the metal oxidation state, the photoexcited system relaxes through a cascade of excited spin states leading to formation of a high spin state, which in the case of the haem is a domed porphyrin.
- Subjects :
- carbon-monoxide
molecular-dynamics
resolved resonance raman
nitric-oxide
transient absorption
x-ray emission spectroscopy
General Medicine
General Chemistry
x-ray absorption spectroscopy
structural dynamics
heam proteins
cytochrome-c
protein excited state dynamics
ultrafast dynamics
hydrogen-sulfide
geminate recombination
excited-state
Subjects
Details
- ISSN :
- 26732424 and 00094293
- Volume :
- 76
- Database :
- OpenAIRE
- Journal :
- CHIMIA
- Accession number :
- edsair.doi.dedup.....76ba103c9be8d501a87c4504bfdface1
- Full Text :
- https://doi.org/10.2533/chimia.2022.538