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An anti-settling sample delivery instrument for serial femtosecond crystallography

MPS-Authors
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Lomb,  Lukas
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

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Steinbrener,  Jan
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

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Beisel,  Daniel
Department of Biomedical Optics, Max Planck Institute for Medical Research, Max Planck Society;

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Berndt,  Daniel
Department of Biomedical Optics, Max Planck Institute for Medical Research, Max Planck Society;

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Kieser,  Christian
Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society;

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Lukat,  Martin
Department of Biomedical Optics, Max Planck Institute for Medical Research, Max Planck Society;

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Neef,  Niklas
Department of Biomedical Optics, Max Planck Institute for Medical Research, Max Planck Society;

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

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Citation

Lomb, L., Steinbrener, J., Bari, S., Beisel, D., Berndt, D., Kieser, C., et al. (2012). An anti-settling sample delivery instrument for serial femtosecond crystallography. Journal of Applied Crystallography, 45(4), 674-678. doi:10.1107/S0021889812024557.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0024-1E28-8
Abstract
Serial femtosecond crystallography (SFX) using X−ray free−electron laser (FEL) sources has the potential to determine the structures of macromolecules beyond the limitation of radiation damage and without the need for crystals of sufficient size for conventional crystallography. In SFX, a liquid microjet is used to inject randomly oriented crystals suspended in their storage solution into the FEL beam. Settling of crystals in the reservoir prior to the injection has been found to complicate the data collection. This article details the development of an antisettling sample delivery instrument based on a rotating syringe pump, capable of producing flow rates and liquid pressures necessary for the operation of the injector. The device has been used successfully with crystals of different proteins, with crystal sizes smaller than 20 mm. Even after hours of continuous operation, no significant impairment of the experiments due to sample settling was observed. This article describes the working principle of the instrument and sets it in context with regard to the experimental conditions used for SFX. Hit rates for longer measuring periods are compared with and without the instrument operating. Two versions of the instrument have been developed, which both deliver sample at a constant flow rate but which differ in their minimum liquid flow rates and maximum pressures