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Single-molecule Detection of Ultrafast Biomolecular Dynamics with Nanophotonics.
Nüesch, Mark F; Ivanovic, Milos T; Claude, Jean-Benoît; Nettels, Daniel; Best, Robert B; Wenger, Jérôme; Schuler, Benjamin.
Afiliação
  • Nüesch MF; Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
  • Ivanovic MT; Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
  • Claude JB; Aix Marseille Univ, CNRS, Centrale Marseille, Institut Fresnel, 13013 Marseille, France.
  • Nettels D; Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
  • Best RB; Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0520, United States.
  • Wenger J; Aix Marseille Univ, CNRS, Centrale Marseille, Institut Fresnel, 13013 Marseille, France.
  • Schuler B; Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
J Am Chem Soc ; 144(1): 52-56, 2022 01 12.
Article em En | MEDLINE | ID: mdl-34970909
Single-molecule Förster resonance energy transfer (FRET) is a versatile technique for probing the structure and dynamics of biomolecules even in heterogeneous ensembles. However, because of the limited fluorescence brightness per molecule and the relatively long fluorescence lifetimes, probing ultrafast structural dynamics in the nanosecond time scale has thus far been very challenging. Here, we demonstrate that nanophotonic fluorescence enhancement in zero-mode waveguides enables measurements of previously inaccessible low-nanosecond dynamics by dramatically improving time resolution and reduces data acquisition times by more than an order of magnitude. As a prototypical example, we use this approach to probe the dynamics of a short intrinsically disordered peptide that were previously inaccessible with single-molecule FRET measurements. We show that we are now able to detect the low-nanosecond correlations in this peptide, and we obtain a detailed interpretation of the underlying distance distributions and dynamics in conjunction with all-atom molecular dynamics simulations, which agree remarkably well with the experiments. We expect this combined approach to be widely applicable to the investigation of very rapid biomolecular dynamics.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transferência Ressonante de Energia de Fluorescência Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Am Chem Soc Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transferência Ressonante de Energia de Fluorescência Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Am Chem Soc Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça
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