Objective
X-ray photons carry sufficient energy to interact with molecular core-shells electrons. Accessible for decades in the energy domain, the resulting core-excited states (CES) can now be observed in the time domain using attosecond (10-18 s) spectroscopy. These states are important as they govern the lineshapes in all x-ray spectroscopies. Here, we propose to first investigate and then manipulate the CES time evolution in solvated biomolecules in order to reveal key chemical information i.e. solute-solvent interactions, local symmetries and
chiral fields.
CES lifetimes dictate the emission of secondary electrons active in radiotherapy. By observing the effect of solute-solvent interactions on CES we will be able to achieve a better understanding of the first molecular mechanisms of radiotherapy.
CES are also a subtle probe of the absorbing atoms bonding environment. CES line splittings are lost in conventional x-ray spectroscopy due to homogenous broadening. We developed a technique based on the laser manipulation of CES capable of producing lineshapes up to an order of magnitude below the spectroscopys lifetime broadening and revealing core-level splitting. We will employ this approach to observe core-level splitting in solvated amino acids and metalloproteins and will use this new information to reveal the binding geometry of ligands with unprecedented accuracy.
Finally, we will show how one can use nonlinear optics with attosecond pulses to reveal the chirality of the field surrounding sulphur and phosphorus atoms in biological samples. X-ray excitation localizes the point of view on the chiral field to a single atom. This perspective will allow us to examine the chiral landscape near the target atom. Here, chirality due to a single chiral centre will be probed in L-cysteine while the chirality due to the macromolecular arrangement will be measured in DNA helixes.
Our proposal brings attoscience techniques in the investigation field of large solvated systems.
Fields of science (EuroSciVoc)
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques.
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques.
- natural sciencesphysical sciencesopticslaser physics
- natural sciencesphysical sciencestheoretical physicsparticle physicsphotons
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Programme(s)
- HORIZON.1.1 - European Research Council (ERC) Main Programme
Topic(s)
Funding Scheme
HORIZON-ERC - HORIZON ERC GrantsHost institution
75015 PARIS 15
France