Ultrafast self-gating Bragg diffraction of exploding nanocrystals in an X-ray laser
Optics Express
|April 4, 2015
Summary
Femtosecond X-ray lasers used for protein structure determination cause damage that limits imaging. Ultrafast ionization and atomic displacement degrade diffraction, with effects varying by intensity and resolution.
Area of Science:
- Structural biology
- Ultrafast X-ray science
Background:
- Intense femtosecond X-ray lasers are crucial for determining the structure of crystalline proteins.
- Damage processes during X-ray exposure can lead to loss of structural coherence, limiting imaging resolution and time scales.
Purpose of the Study:
- To investigate the nonthermal damage dynamics in crystalline proteins exposed to femtosecond X-ray lasers.
- To understand how ionization and atomic displacement affect Bragg diffraction and ultrafast imaging.
Main Methods:
- Utilizing a nonthermal description for damage dynamics.
- Calculating ultrafast ionization and subsequent atomic displacement.
- Analyzing the intensity and resolution dependence of diffraction degradation.
Main Results:
- Damage processes degrade Bragg diffraction on femtosecond time scales, gating ultrafast imaging.
- At high intensities, ionization affects low-resolution information first.
- At lower intensities, atomic displacement impacts high-resolution information.
Conclusions:
- Pulse length is not a limiting factor for X-ray imaging if X-ray flux is sufficient.
- Understanding damage mechanisms is key to optimizing ultrafast protein structure determination.
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