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Journal Article

Low-dose fixed-target serial synchrotron crystallography

MPS-Authors
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Schulz,  Eike-Christian
Miller Group, Atomically Resolved Dynamics Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

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Miller,  R. J. Dwayne
Miller Group, Atomically Resolved Dynamics Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
Departments of Chemistry and Physics, University of Toronto, King's College Circle;

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Müller-Werkmeister,  Henrike
Miller Group, Atomically Resolved Dynamics Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

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Citation

Owen, R. L., Axford, D., Sherrell, D. A., Kuo, A., Ernst, O. P., Schulz, E.-C., et al. (2017). Low-dose fixed-target serial synchrotron crystallography. Acta Crystallographica Section D: Structural Biology, 73, 373-378. doi:10.1107/S2059798317002996.


Cite as: http://hdl.handle.net/11858/00-001M-0000-002C-E821-F
Abstract
The development of serial crystallography has been driven by the sample requirements imposed by X-ray free-electron lasers. Serial techniques are now being exploited at synchrotrons. Using a fixed-target approach to high-throughput serial sampling, it is demonstrated that high-quality data can be collected from myoglobin crystals, allowing room-temperature, low-dose structure determination. The combination of fixed-target arrays and a fast, accurate translation system allows high-throughput serial data collection at high hit rates and with low sample consumption.