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Real-time tracking of protein unfolding with time-resolved x-ray solution scattering.
Henry, L; Panman, M R; Isaksson, L; Claesson, E; Kosheleva, I; Henning, R; Westenhoff, S; Berntsson, O.
Afiliación
  • Henry L; Department of Chemistry and Molecular Biology, University of Gothenburg, 40530 Gothenburg, Sweden.
  • Panman MR; Department of Chemistry and Molecular Biology, University of Gothenburg, 40530 Gothenburg, Sweden.
  • Isaksson L; Department of Chemistry and Molecular Biology, University of Gothenburg, 40530 Gothenburg, Sweden.
  • Claesson E; Department of Chemistry and Molecular Biology, University of Gothenburg, 40530 Gothenburg, Sweden.
  • Kosheleva I; Center for Advanced Radiation Sources, The University of Chicago, Chicago, Illinois 60637, USA.
  • Henning R; Center for Advanced Radiation Sources, The University of Chicago, Chicago, Illinois 60637, USA.
  • Westenhoff S; Department of Chemistry and Molecular Biology, University of Gothenburg, 40530 Gothenburg, Sweden.
Struct Dyn ; 7(5): 054702, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32984436
The correct folding of proteins is of paramount importance for their function, and protein misfolding is believed to be the primary cause of a wide range of diseases. Protein folding has been investigated with time-averaged methods and time-resolved spectroscopy, but observing the structural dynamics of the unfolding process in real-time is challenging. Here, we demonstrate an approach to directly reveal the structural changes in the unfolding reaction. We use nano- to millisecond time-resolved x-ray solution scattering to probe the unfolding of apomyoglobin. The unfolding reaction was triggered using a temperature jump, which was induced by a nanosecond laser pulse. We demonstrate a new strategy to interpret time-resolved x-ray solution scattering data, which evaluates ensembles of structures obtained from molecular dynamics simulations. We find that apomyoglobin passes three states when unfolding, which we characterize as native, molten globule, and unfolded. The molten globule dominates the population under the conditions investigated herein, whereas native and unfolded structures primarily contribute before the laser jump and 30 µs after it, respectively. The molten globule retains much of the native structure but shows a dynamic pattern of inter-residue contacts. Our study demonstrates a new strategy to directly observe structural changes over the cause of the unfolding reaction, providing time- and spatially resolved atomic details of the folding mechanism of globular proteins.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Struct Dyn Año: 2020 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Struct Dyn Año: 2020 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Estados Unidos