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Structures of multisubunit membrane complexes with the CRYO ARM 200.

Christoph GerleJun-Ichi KishikawaTomoko YamaguchiAtsuko NakanishiOrkun ÇoruhFumiaki MakinoTomoko MiyataAkihiro KawamotoKen YokoyamaKeiichi NambaGenji KurisuTakayuki Kato
Published in: Microscopy (Oxford, England) (2022)
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 lipopolysaccharide peptidoglycan ring (LP ring) from Salmonella enterica.
Keyphrases
  • electron microscopy
  • molecularly imprinted
  • solid phase extraction
  • high resolution
  • inflammatory response
  • deep learning
  • immune response
  • machine learning
  • electron transfer
  • bacillus subtilis