@article{11648,
  abstract     = {Progress in structural membrane biology has been significantly accelerated by the ongoing 'Resolution Revolution' in cryo electron microscopy (cryo-EM). In particular, structure determination by single particle analysis has evolved into the most powerful method for atomic model building of multisubunit membrane protein complexes. This has created an ever increasing demand in cryo-EM machine time, which to satisfy is in need of new and affordable cryo electron microscopes. Here, we review our experience in using the JEOL CRYO ARM 200 prototype for the structure determination by single particle analysis of three different multisubunit membrane complexes: the Thermus thermophilus V-type ATPase VO complex, the Thermosynechococcus elongatus photosystem I monomer and the flagellar motor LP-ring from Salmonella enterica.},
  author       = {Gerle, Christoph and Kishikawa, Jun-ichi and Yamaguchi, Tomoko and Nakanishi, Atsuko and Çoruh, Mehmet Orkun and Makino, Fumiaki and Miyata, Tomoko and Kawamoto, Akihiro and Yokoyama, Ken and Namba, Keiichi and Kurisu, Genji and Kato, Takayuki},
  issn         = {2050-5701},
  journal      = {Microscopy},
  keywords     = {Radiology, Nuclear Medicine and imaging, Instrumentation, Structural Biology},
  number       = {5},
  pages        = {249--261},
  publisher    = {Oxford University Press},
  title        = {{Structures of multisubunit membrane complexes with the CRYO ARM 200}},
  doi          = {10.1093/jmicro/dfac037},
  volume       = {71},
  year         = {2022},
}