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FoldAffinity: binding affinities from nDSF experiments.
Niebling, Stephan; Burastero, Osvaldo; Bürgi, Jérôme; Günther, Christian; Defelipe, Lucas A; Sander, Simon; Gattkowski, Ellen; Anjanappa, Raghavendra; Wilmanns, Matthias; Springer, Sebastian; Tidow, Henning; García-Alai, María.
Afiliación
  • Niebling S; European Molecular Biology Laboratory - Hamburg Outstation, Notkestr. 85, Hamburg, 22607, Germany. stephan.niebling@embl-hamburg.de.
  • Burastero O; Centre for Structural Systems Biology, Notkestrasse 85, 22607, Hamburg, Germany. stephan.niebling@embl-hamburg.de.
  • Bürgi J; European Molecular Biology Laboratory - Hamburg Outstation, Notkestr. 85, Hamburg, 22607, Germany.
  • Günther C; Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Intendente Güiraldes 2620, Buenos Aires, Argentina.
  • Defelipe LA; IQUIBICEN-UBA/CONICET, Intendente Güiraldes, 2620, Buenos Aires, Argentina.
  • Sander S; European Molecular Biology Laboratory - Hamburg Outstation, Notkestr. 85, Hamburg, 22607, Germany.
  • Gattkowski E; European Molecular Biology Laboratory - Hamburg Outstation, Notkestr. 85, Hamburg, 22607, Germany.
  • Anjanappa R; European Molecular Biology Laboratory - Hamburg Outstation, Notkestr. 85, Hamburg, 22607, Germany.
  • Wilmanns M; Hamburg Advanced Research Centre for Bioorganic Chemistry (HARBOR) & Department of Chemistry, Institute for Biochemistry and Molecular Biology, University of Hamburg, Luruper Chaussee 149, 22761, Hamburg, Germany.
  • Springer S; Hamburg Advanced Research Centre for Bioorganic Chemistry (HARBOR) & Department of Chemistry, Institute for Biochemistry and Molecular Biology, University of Hamburg, Luruper Chaussee 149, 22761, Hamburg, Germany.
  • Tidow H; Department of Life Sciences and Chemistry, Jacobs University Bremen, 28759, Bremen, Germany.
  • García-Alai M; European Molecular Biology Laboratory - Hamburg Outstation, Notkestr. 85, Hamburg, 22607, Germany.
Sci Rep ; 11(1): 9572, 2021 05 05.
Article en En | MEDLINE | ID: mdl-33953265
Differential scanning fluorimetry (DSF) using the inherent fluorescence of proteins (nDSF) is a popular technique to evaluate thermal protein stability in different conditions (e.g. buffer, pH). In many cases, ligand binding increases thermal stability of a protein and often this can be detected as a clear shift in nDSF experiments. Here, we evaluate binding affinity quantification based on thermal shifts. We present four protein systems with different binding affinity ligands, ranging from nM to high µM. Our study suggests that binding affinities determined by isothermal analysis are in better agreement with those from established biophysical techniques (ITC and MST) compared to apparent Kds obtained from melting temperatures. In addition, we describe a method to optionally fit the heat capacity change upon unfolding ([Formula: see text]) during the isothermal analysis. This publication includes the release of a web server for easy and accessible application of isothermal analysis to nDSF data.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Sci Rep Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Sci Rep Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido