Your browser doesn't support javascript.
loading
Modular Imaging Scaffold for Single-Particle Electron Microscopy.
Aissaoui, Nesrine; Lai-Kee-Him, Josephine; Mills, Allan; Declerck, Nathalie; Morichaud, Zakia; Brodolin, Konstantin; Baconnais, Sonia; Le Cam, Eric; Charbonnier, Jean Baptiste; Sounier, Rémy; Granier, Sébastien; Ropars, Virginie; Bron, Patrick; Bellot, Gaetan.
Afiliação
  • Aissaoui N; Centre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, F-34000 Montpellier, France.
  • Lai-Kee-Him J; Université de Montpellier, F-34000 Montpellier, France.
  • Mills A; Centre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, F-34000 Montpellier, France.
  • Declerck N; Université de Montpellier, F-34000 Montpellier, France.
  • Morichaud Z; Centre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, F-34000 Montpellier, France.
  • Brodolin K; Université de Montpellier, F-34000 Montpellier, France.
  • Baconnais S; Centre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, F-34000 Montpellier, France.
  • Le Cam E; Université de Montpellier, F-34000 Montpellier, France.
  • Charbonnier JB; Departement MICA, INRA, 78352 Jouy-en-Josas, France.
  • Sounier R; Université de Montpellier, F-34000 Montpellier, France.
  • Granier S; IRIM, CNRS, Université Montpellier, 1919 Route de Mende, 34293 Montpellier, France.
  • Ropars V; Université de Montpellier, F-34000 Montpellier, France.
  • Bron P; IRIM, CNRS, Université Montpellier, 1919 Route de Mende, 34293 Montpellier, France.
  • Bellot G; Signalisations, Noyaux et Innovations en Cancérologie, UMR 8126, CNRS, Université Paris-Sud, Gustave Roussy, Université Paris-Saclay, 94800 Villejuif, France.
ACS Nano ; 15(3): 4186-4196, 2021 03 23.
Article em En | MEDLINE | ID: mdl-33586425
ABSTRACT
Technological breakthroughs in electron microscopy (EM) have made it possible to solve structures of biological macromolecular complexes and to raise novel challenges, specifically related to sample preparation and heterogeneous macromolecular assemblies such as DNA-protein, protein-protein, and membrane protein assemblies. Here, we built a V-shaped DNA origami as a scaffolding molecular system to template proteins at user-defined positions in space. This template positions macromolecular assemblies of various sizes, juxtaposes combinations of biomolecules into complex arrangements, isolates biomolecules in their active state, and stabilizes membrane proteins in solution. In addition, the design can be engineered to tune DNA mechanical properties by exerting a controlled piconewton (pN) force on the molecular system and thus adapted to characterize mechanosensitive proteins. The binding site can also be specifically customized to accommodate the protein of interest, either interacting spontaneously with DNA or through directed chemical conjugation, increasing the range of potential targets for single-particle EM investigation. We assessed the applicability for five different proteins. Finally, as a proof of principle, we used RNAP protein to validate the approach and to explore the compatibility of the template with cryo-EM sample preparation.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Imagem Individual de Molécula Idioma: En Revista: ACS Nano Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Imagem Individual de Molécula Idioma: En Revista: ACS Nano Ano de publicação: 2021 Tipo de documento: Article