Your browser doesn't support javascript.
loading
Deep Mutational Scans as a Guide to Engineering High Affinity T Cell Receptor Interactions with Peptide-bound Major Histocompatibility Complex.
Harris, Daniel T; Wang, Ningyan; Riley, Timothy P; Anderson, Scott D; Singh, Nishant K; Procko, Erik; Baker, Brian M; Kranz, David M.
Afiliación
  • Harris DT; From the Department of Biochemistry, University of Illinois, Urbana, Illinois 61801 and.
  • Wang N; From the Department of Biochemistry, University of Illinois, Urbana, Illinois 61801 and.
  • Riley TP; the Department of Chemistry and Biochemistry and the Harper Cancer Research Institute, University of Notre Dame, South Bend, Indiana 46557.
  • Anderson SD; From the Department of Biochemistry, University of Illinois, Urbana, Illinois 61801 and.
  • Singh NK; the Department of Chemistry and Biochemistry and the Harper Cancer Research Institute, University of Notre Dame, South Bend, Indiana 46557.
  • Procko E; From the Department of Biochemistry, University of Illinois, Urbana, Illinois 61801 and.
  • Baker BM; the Department of Chemistry and Biochemistry and the Harper Cancer Research Institute, University of Notre Dame, South Bend, Indiana 46557.
  • Kranz DM; From the Department of Biochemistry, University of Illinois, Urbana, Illinois 61801 and. Electronic address: d-kranz@illinois.edu.
J Biol Chem ; 291(47): 24566-24578, 2016 Nov 18.
Article en En | MEDLINE | ID: mdl-27681597
Proteins are often engineered to have higher affinity for their ligands to achieve therapeutic benefit. For example, many studies have used phage or yeast display libraries of mutants within complementarity-determining regions to affinity mature antibodies and T cell receptors (TCRs). However, these approaches do not allow rapid assessment or evolution across the entire interface. By combining directed evolution with deep sequencing, it is now possible to generate sequence fitness landscapes that survey the impact of every amino acid substitution across the entire protein-protein interface. Here we used the results of deep mutational scans of a TCR-peptide-MHC interaction to guide mutational strategies. The approach yielded stable TCRs with affinity increases of >200-fold. The substitutions with the greatest enrichments based on the deep sequencing were validated to have higher affinity and could be combined to yield additional improvements. We also conducted in silico binding analyses for every substitution to compare them with the fitness landscape. Computational modeling did not effectively predict the impacts of mutations distal to the interface and did not account for yeast display results that depended on combinations of affinity and protein stability. However, computation accurately predicted affinity changes for mutations within or near the interface, highlighting the complementary strengths of computational modeling and yeast surface display coupled with deep mutational scanning for engineering high affinity TCRs.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Simulación por Computador / Receptores de Antígenos de Linfocitos T / Modelos Moleculares / Antígeno HLA-A2 Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: J Biol Chem Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Péptidos / Simulación por Computador / Receptores de Antígenos de Linfocitos T / Modelos Moleculares / Antígeno HLA-A2 Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: J Biol Chem Año: 2016 Tipo del documento: Article