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@ARTICLE{Roedig:328901,
      author       = {Roedig, Philip and Ginn, Helen and Pakendorf, Tim and
                      Sutton, Geoff and Harlos, Karl and Walter, Thomas S and
                      Meyer, Jan and Fischer, Pontus and Duman, Ramona and
                      Vartiainen, Ismo and Reime, Bernd and Warmer, Martin and
                      Brewster, Aaron S and Young, Iris D and Michels-Clark, Tara
                      and Sauter, Nicholas K and Kotecha, Abhay and Kelly, James
                      and Rowlands, David J and Sikorsky, Marcin and Nelson, Silke
                      and Damiani, Daniel S and Alonso-Mori, Roberto and Ren,
                      Jingshan and Fry, Elizabeth E and David, Christian and
                      Stuart, David I m and Wagner, Armin and Meents, Alke},
      title        = {{H}igh-speed fixed-target serial virus crystallography},
      journal      = {Nature methods},
      volume       = {14},
      issn         = {1548-7091},
      address      = {London [u.a.] Nature Publishing Group},
      publisher    = {Nature Publishing Group},
      reportid     = {PUBDB-2017-05548},
      pages        = {805-810},
      year         = {2017},
      note         = {(c) Nature America; Post referee fulltext in progress 2;
                      Embargo 6 months from publication},
      abstract     = {We report a method for serial X-ray crystallography at
                      X-ray free-electron lasers (XFELs), which allows for full
                      use of the current 120-Hz repetition rate of the Linear
                      Coherent Light Source (LCLS). Using a micropatterned silicon
                      chip in combination with the high-speed Roadrunner
                      goniometer for sample delivery, we were able to determine
                      the crystal structures of the picornavirus bovine
                      enterovirus 2 (BEV2) and the cytoplasmic polyhedrosis virus
                      type 18 polyhedrin, with total data collection times of less
                      than 14 and 10 min, respectively. Our method requires only
                      micrograms of sample and should therefore broaden the
                      applicability of serial femtosecond crystallography to
                      challenging projects for which only limited sample amounts
                      are available. By synchronizing the sample exchange to the
                      XFEL repetition rate, our methodallows for most efficient
                      use of the limited beam time available at XFELs and should
                      enable a substantial increase in sample throughput at these
                      facilities.},
      cin          = {FS-PS / FS-PE / FS-CFEL-1},
      ddc          = {570},
      cid          = {I:(DE-H253)FS-PS-20131107 / I:(DE-H253)FS-PE-20120731 /
                      I:(DE-H253)FS-CFEL-1-20120731},
      pnm          = {6215 - Soft Matter, Health and Life Sciences (POF3-621) /
                      VH-VI-403 - In-Situ Nano-Imaging of Biological and Chemical
                      Processes $(2015_IFV-VH-VI-403)$ / EUCALL - European Cluster
                      of Advanced Laser Light Sources (654220)},
      pid          = {G:(DE-HGF)POF3-6215 / $G:(DE-HGF)2015_IFV-VH-VI-403$ /
                      G:(EU-Grant)654220},
      experiment   = {EXP:(DE-MLZ)External-20140101},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:28628129},
      UT           = {WOS:000406493800020},
      doi          = {10.1038/nmeth.4335},
      url          = {https://bib-pubdb1.desy.de/record/328901},
}