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Insertion and activation of functional Bacteriorhodopsin in a floating bilayer.
Mukhina, Tetiana; Gerelli, Yuri; Hemmerle, Arnaud; Koutsioubas, Alexandros; Kovalev, Kirill; Teulon, Jean-Marie; Pellequer, Jean-Luc; Daillant, Jean; Charitat, Thierry; Fragneto, Giovanna.
Affiliation
  • Mukhina T; Institut Laue-Langevin, 71 av.des Martyrs, BP 156, 38042 Grenoble Cedex, France; Institut Charles Sadron, Université de Strasbourg, CNRS, UPR 22, 67034 Strasbourg, France.
  • Gerelli Y; Institut Laue-Langevin, 71 av.des Martyrs, BP 156, 38042 Grenoble Cedex, France; Marche Polytechnic University, Department of Life and Environmental Sciences, Via Brecce Bianche, 60131 Ancona, Italy.
  • Hemmerle A; Synchrotron SOLEIL, L'Orme des Merisiers, Saint-Aubin, BP 48, F-91192 Gif-sur-Yvette Cedex, France.
  • Koutsioubas A; Jülich Centre for Neutron Science (JCNS) at Heinz Maier-Leibnitz Zentrum (MLZ), Forschungszentrum Jülich GmbH, Lichtenbergstr. 1, 85748 Garching, Germany.
  • Kovalev K; Univ. Grenoble Alpes, CEA, CNRS, Institut de Biologie Structurale (IBS), F-38000 Grenoble, France; Institute of Biological Information Processing (IBI-7), Structural Biochemistry, Forschungszentrum Jülich, 52428, Wilhelm-Johnen-Straße, Jülich, Germany; Jülich Centre for Neutron Science (JCNS) at Hei
  • Teulon JM; Univ. Grenoble Alpes, CEA, CNRS, Institut de Biologie Structurale (IBS), F-38000 Grenoble, France.
  • Pellequer JL; Univ. Grenoble Alpes, CEA, CNRS, Institut de Biologie Structurale (IBS), F-38000 Grenoble, France.
  • Daillant J; Synchrotron SOLEIL, L'Orme des Merisiers, Saint-Aubin, BP 48, F-91192 Gif-sur-Yvette Cedex, France.
  • Charitat T; Institut Charles Sadron, Université de Strasbourg, CNRS, UPR 22, 67034 Strasbourg, France.
  • Fragneto G; Institut Laue-Langevin, 71 av.des Martyrs, BP 156, 38042 Grenoble Cedex, France.
J Colloid Interface Sci ; 597: 370-382, 2021 Sep.
Article de En | MEDLINE | ID: mdl-33894545
ABSTRACT
The proton pump transmembrane protein bacteriorhodopsin was successfully incorporated into planar floating lipid bilayers in gel and fluid phases, by applying a detergent-mediated incorporation method. The method was optimized on single supported bilayers by using quartz crystal microbalance, atomic force and fluorescence microscopy techniques. Neutron and X-ray reflectometry were used on both single and floating bilayers with the aim of determining the structure and composition of this membrane-protein system before and after protein reconstitution at sub-nanometer resolution. Lipid bilayer integrity and protein activity were preserved upon the reconstitution process. Reversible structural modifications of the membrane, induced by the bacteriorhodopsin functional activity triggered by visible light, were observed and characterized at the nanoscale.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Bactériorhodopsines Langue: En Journal: J Colloid Interface Sci Année: 2021 Type de document: Article Pays d'affiliation: France

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Bactériorhodopsines Langue: En Journal: J Colloid Interface Sci Année: 2021 Type de document: Article Pays d'affiliation: France
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