Kilohertz droplet-on-demand serial femtosecond crystallography at the European XFEL station FXE

Author:

Perrett Samuel1ORCID,Fadini Alisia1,Hutchison Christopher D. M.12ORCID,Bhattacharya Sayantan1ORCID,Morrison Cade1ORCID,Turkot Oleksii3,Jakobsen Mads Bregenholt4ORCID,Größler Michael4,Licón-Saláiz José4,Griese Florian456,Flewett Samuel4,Valerio Joana3,Schulz Joachim3ORCID,Biednov Mykola3,Jiang Yifeng3ORCID,Han Huijong3,Yousef Hazem3,Khakhulin Dmitry3,Milne Christopher3ORCID,Barty Anton4,van Thor Jasper J.1ORCID

Affiliation:

1. Department of Life Sciences, Faculty of Natural Sciences, Imperial College London 1 , London SW7 2AZ, United Kingdom

2. Central Laser Facility 2 , Rutherford Appleton Laboratory, Didcot OX11 0QX, United Kingdom

3. European XFEL 3 , Holzkoppel 4, 22869 Schenefeld, Germany

4. Center for Data and Computing in Natural Sciences (CDCS) 4 , Notkestrasse 10, D-22607 Hamburg, Germany

5. Section for Biomedical Imaging, University Medical Center Hamburg-Eppendorf 5 , D-20246 Hamburg, Germany

6. Institute for Biomedical Imaging, Hamburg University of Technology 6 , D-21073 Hamburg, Germany

Abstract

X-ray Free Electron Lasers (XFELs) allow the collection of high-quality serial femtosecond crystallography data. The next generation of megahertz superconducting FELs promises to drastically reduce data collection times, enabling the capture of more structures with higher signal-to-noise ratios and facilitating more complex experiments. Currently, gas dynamic virtual nozzles (GDVNs) stand as the sole delivery method capable of best utilizing the repetition rate of megahertz sources for crystallography. However, their substantial sample consumption renders their use impractical for many protein targets in serial crystallography experiments. Here, we present a novel application of a droplet-on-demand injection method, which allowed operation at 47 kHz at the European XFEL (EuXFEL) by tailoring a multi-droplet injection scheme for each macro-pulse. We demonstrate a collection rate of 150 000 indexed patterns per hour. We show that the performance and effective data collection rate are comparable to GDVN, with a sample consumption reduction of two orders of magnitude. We present lysozyme crystallographic data using the Large Pixel Detector at the femtosecond x-ray experiment endstation. Significant improvement of the crystallographic statistics was made by correcting for a systematic drift of the photon energy in the EuXFEL macro-pulse train, which was characterized from indexing the individual frames in the pulse train. This is the highest resolution protein structure collected and reported at the EuXFEL at 1.38 Å resolution.

Funder

Biotechnology and Biological Sciences Research Council

Engineering and Physical Sciences Research Council

Publisher

AIP Publishing

Reference69 articles.

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