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Journal Article

Towards phasing using high X-ray intensity

MPS-Authors
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Barends,  Thomas R. M.
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons117990

Botha,  Sabine
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons117878

Doak,  Bruce
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons117928

Nass,  Karol
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons95345

Shoeman,  Robert L.
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons95189

Schlichting,  Ilme
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

External Resource

http://journals.iucr.org/m/issues/2015/06/00/gq5004/gq5004.pdf
(Any fulltext)

http://dx.doi.org/10.1107/S2052252515014049
(Any fulltext)

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Citation

Galli, L., Son, S.-K., Barends, T. R. M., White, T. A., Barty, A., Botha, S., et al. (in press). Towards phasing using high X-ray intensity. IUCrJ, 2(6), 627-634. doi:10.1107/S2052252515014049.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0029-0145-A
Abstract
Analysis of serial femtosecond crystallography data collected at the Linac Coherent Light Source using two distinct photon fluxes shows different degrees of ionization of Gd atoms bound to a lysozyme protein, due to electronic damage processes. The charge contrast on the heavy atoms is quantified using difference Fourier maps, and the way in which this could be applied to phasing is discussed.