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Characterization of heterogeneity in nanodisc samples using Feret signatures.
Vilela, Fernando; Bezault, Armel; Rodriguez de Francisco, Borja; Sauvanet, Cécile; Xu, Xiao-Ping; Swift, Mark F; Yao, Yong; Marrasi, Francesca M; Hanein, Dorit; Volkmann, Niels.
Afiliação
  • Vilela F; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Studies of Macromolecular Machines in Cellulo Unit, F-75015 Paris, France; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Image Analysis Unit, F-75015 Paris, France.
  • Bezault A; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Studies of Macromolecular Machines in Cellulo Unit, F-75015 Paris, France; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Image Analysis Unit, F-75015 Paris, France.
  • Rodriguez de Francisco B; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Studies of Macromolecular Machines in Cellulo Unit, F-75015 Paris, France; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Image Analysis Unit, F-75015 Paris, France.
  • Sauvanet C; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Studies of Macromolecular Machines in Cellulo Unit, F-75015 Paris, France; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Image Analysis Unit, F-75015 Paris, France.
  • Xu XP; Scintillon Institute, San Diego, CA, USA.
  • Swift MF; Scintillon Institute, San Diego, CA, USA.
  • Yao Y; Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
  • Marrasi FM; Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
  • Hanein D; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Studies of Macromolecular Machines in Cellulo Unit, F-75015 Paris, France; Scintillon Institute, San Diego, CA, USA. Electronic address: dorit@scintillon.org.
  • Volkmann N; Institut Pasteur, Université Paris Cité, CNRS UMR3528, Structural Image Analysis Unit, F-75015 Paris, France. Electronic address: niels.volkmann@pasteur.fr.
J Struct Biol ; 214(4): 107916, 2022 12.
Article em En | MEDLINE | ID: mdl-36332745
ABSTRACT
Nanodiscs have become a popular tool in structure determination of membrane proteins using cryogenic electron microscopy and single particle analysis. However, the structure determination of small membrane proteins remains challenging. When the embedded protein is in the same size range as the nanodisc, the nanodisc can significantly contribute to the alignment and classification during the structure determination process. In those cases, it is crucial to minimize the heterogeneity in the nanodisc preparations to assure maximum accuracy in the classification and alignment steps of single particle analysis. Here, we introduce a new in-silico method for the characterization of nanodisc samples that is based on analyzing the Feret diameter distribution of their particle projection as imaged in the electron microscope. We validated the method with comprehensive simulation studies and show that Feret signatures can detect subtle differences in nanodisc morphologies and composition that might otherwise go unnoticed. We used the method to identify a specific biochemical nanodisc preparation with low size variations, allowing us to obtain a structure of the 23-kDa single-span membrane protein Bcl-xL while embedded in a nanodisc. Feret signature analysis can steer experimental data collection strategies, allowing more efficient use of high-end data collection hardware, as well as image analysis investments in studies where nanodiscs significantly contribute to the total volume of the full molecular species.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Struct Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Struct Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França