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Membrane mimetic systems in CryoEM: keeping membrane proteins in their native environment.
Autzen, Henriette E; Julius, David; Cheng, Yifan.
Afiliação
  • Autzen HE; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94143, USA; Department of Molecular Biology and Genetics, Aarhus University, 8000 Aarhus, Denmark.
  • Julius D; Department of Physiology, University of California, San Francisco, CA 94143, USA. Electronic address: David.Julis@ucsf.edu.
  • Cheng Y; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, University of California, San Francisco, CA 94143, USA. Electronic address: Yifan.Cheng@ucsf.edu.
Curr Opin Struct Biol ; 58: 259-268, 2019 10.
Article em En | MEDLINE | ID: mdl-31279500
ABSTRACT
Advances in electron microscopes, detectors and data processing algorithms have greatly facilitated the structural determination of many challenging integral membrane proteins that have been evasive to crystallization. These breakthroughs facilitate the application and development of various membrane protein solubilization approaches for structural studies, including reconstitution into lipid nanoparticles. In this review, we discuss various approaches for preparing transmembrane proteins for structural determination with single-particle electron cryo microscopy (cryoEM).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microscopia Crioeletrônica / Proteínas de Membrana / Membranas Artificiais Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microscopia Crioeletrônica / Proteínas de Membrana / Membranas Artificiais Idioma: En Ano de publicação: 2019 Tipo de documento: Article