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Decoding Biomineralization: Interaction of a Mad10-Derived Peptide with Magnetite Thin Films.
Pohl, Anna; Berger, Florian; Sullan, Ruby M A; Valverde-Tercedor, Carmen; Freindl, Kinga; Spiridis, Nika; Lefèvre, Christopher T; Menguy, Nicolas; Klumpp, Stefan; Blank, Kerstin G; Faivre, Damien.
Afiliación
  • Pohl A; Department of Biomaterials , Max Planck Institute of Colloids and Interfaces , Am Mühlenberg 1 , 14476 Potsdam , Germany.
  • Berger F; Mechano(bio)chemistry , Max Planck Institute of Colloids and Interfaces , Am Mühlenberg 1 , 14476 Potsdam , Germany.
  • Sullan RMA; Laboratory of Sensory Neuroscience , The Rockefeller University , 1230 York Avenue , New York 10065 , United States.
  • Valverde-Tercedor C; Mechano(bio)chemistry , Max Planck Institute of Colloids and Interfaces , Am Mühlenberg 1 , 14476 Potsdam , Germany.
  • Freindl K; Department of Biomaterials , Max Planck Institute of Colloids and Interfaces , Am Mühlenberg 1 , 14476 Potsdam , Germany.
  • Spiridis N; Jerzy Haber Institute of Catalysis and Surface Chemistry , Polish Academy of Sciences , Niezapominajek 8 , 30-239 Krakow , Poland.
  • Lefèvre CT; Jerzy Haber Institute of Catalysis and Surface Chemistry , Polish Academy of Sciences , Niezapominajek 8 , 30-239 Krakow , Poland.
  • Menguy N; Aix-Marseille Université , CEA, CNRS, BIAM, 13108 Saint Paul lez Durance , France.
  • Klumpp S; Sorbonne Université , UMR CNRS 7590, IRD. MNHN, Institut de Minéralogie, Physique des Matériaux et Cosmochimie - IMPMC , 4 Place Jussieu , 75005 Paris , France.
  • Blank KG; Department of Theory & Bio-Systems , Max Planck Institute of Colloids and Interfaces , Am Mühlenberg 1 , 14476 Potsdam , Germany.
  • Faivre D; Institute for the Dynamics of Complex Systems , University of Göttingen , Friedrich Hund Platz 1 , 37077 Göttingen , Germany.
Nano Lett ; 19(11): 8207-8215, 2019 11 13.
Article en En | MEDLINE | ID: mdl-31565946
ABSTRACT
Protein-surface interactions play a pivotal role in processes as diverse as biomineralization, biofouling, and the cellular response to medical implants. In biomineralization processes, biomacromolecules control mineral deposition and architecture via complex and often unknown mechanisms. For studying these mechanisms, the formation of magnetite nanoparticles in magnetotactic bacteria has become an excellent model system. Most interestingly, nanoparticle morphologies have been discovered that defy crystallographic rules (e.g., in the species Desulfamplus magnetovallimortis strain BW-1). In certain conditions, this strain mineralizes bullet-shaped magnetite nanoparticles, which exhibit defined (111) crystal faces and are elongated along the [100] direction. We hypothesize that surface-specific protein interactions break the nanoparticle symmetry, inhibiting the growth of certain crystal faces and thereby favoring the growth of others. Screening the genome of BW-1, we identified Mad10 (Magnetosome-associated deep-branching) as a potential magnetite-binding protein. Using atomic force microscope (AFM)-based single-molecule force spectroscopy, we show that a Mad10-derived peptide, which represents the most conserved region of Mad10, binds strongly to (100)- and (111)-oriented single-crystalline magnetite thin films. The peptide-magnetite interaction is thus material- but not crystal-face-specific. It is characterized by broad rupture force distributions that do not depend on the retraction speed of the AFM cantilever. To account for these experimental findings, we introduce a three-state model that incorporates fast rebinding. The model suggests that the peptide-surface interaction is strong in the absence of load, which is a direct result of this fast rebinding process. Overall, our study sheds light on the kinetic nature of peptide-surface interactions and introduces a new magnetite-binding peptide with potential use as a functional coating for magnetite nanoparticles in biotechnological and biomedical applications.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Proteínas Bacterianas / Deltaproteobacteria / Óxido Ferrosoférrico / Magnetosomas Tipo de estudio: Prognostic_studies Idioma: En Revista: Nano Lett Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Proteínas Bacterianas / Deltaproteobacteria / Óxido Ferrosoférrico / Magnetosomas Tipo de estudio: Prognostic_studies Idioma: En Revista: Nano Lett Año: 2019 Tipo del documento: Article País de afiliación: Alemania