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Identification of photocrosslinking peptide ligands by mRNA display.
Wu, Yuteng; Bertran, M Teresa; Joshi, Dhira; Maslen, Sarah L; Hurd, Catherine; Walport, Louise J.
Afiliação
  • Wu Y; Protein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Bertran MT; Department of Chemistry, Molecular Sciences Research Hub, Imperial College London, London, W12 0BZ, UK.
  • Joshi D; Protein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Maslen SL; Chemical Biology, The Francis Crick Institute, London, NW1 1AT, UK.
  • Hurd C; Proteomics, The Francis Crick Institute, London, NW1 1AT, UK.
  • Walport LJ; Protein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
Commun Chem ; 6(1): 103, 2023 May 31.
Article em En | MEDLINE | ID: mdl-37258712
ABSTRACT
Photoaffinity labelling is a promising method for studying protein-ligand interactions. However, obtaining a specific, efficient crosslinker can require significant optimisation. We report a modified mRNA display strategy, photocrosslinking-RaPID (XL-RaPID), and exploit its ability to accelerate the discovery of cyclic peptides that photocrosslink to a target of interest. As a proof of concept, we generated a benzophenone-containing library and applied XL-RaPID screening against a model target, the second bromodomain of BRD3. This crosslinking screening gave two optimal candidates that selectively labelled the target protein in cell lysate. Overall, this work introduces direct photocrosslinking screening as a versatile technique for identifying covalent peptide ligands from mRNA display libraries incorporating reactive warheads.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Commun Chem Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Commun Chem Ano de publicação: 2023 Tipo de documento: Article