Possibility of single biomolecular imaging with coherent amplification of weak scattering X-ray photons
Tsumoru Shintake

TL;DR
This paper proposes a novel holographic method to amplify and detect weak X-ray scattering signals from single biomolecules, enabling high-resolution imaging with potential applications in structural biology.
Contribution
It introduces a new approach combining coherent amplification with holography and phase retrieval to improve single biomolecular imaging with X-ray free electron lasers.
Findings
Amplification of scattered X-ray waves using a gold reference particle.
Potential to collect 10^4 to 10^5 photons in single-shot imaging.
Enhanced phase retrieval for Angstrom-resolution biomolecular images.
Abstract
The number of photons available by coherent X-ray scattering from a single biomolecule is considerably less because of the extremely small elastic-scattering cross-section and low damage threshold. Even with a high X-ray flux of 3 x 10to 12 photons per 100-nm-diameter spot and an ultrashort pulse of 10 fs driven by a future X-ray free electron laser (X-ray FEL), it has been predicted that only a few 100 photons will be available by scattering from a single lysozyme molecule. In this paper I propose a new method: instead of directly observing the photons scattered from the sample, we amplify the scattered waves by superimposing an intense coherent reference pump wave on it and record the resulting interference pattern using a planar X-ray detector, similar to technique followed in holography. Using a nanosized gold particle as a reference pump wave source, we can collect 10 to 4 ~ 10 to…
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