Improving binding affinity and stability of peptide ligands by substituting glycines with D-amino acids.

Details

Serval ID
serval:BIB_348A5320AF5C
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Improving binding affinity and stability of peptide ligands by substituting glycines with D-amino acids.
Journal
Chembiochem
Author(s)
Chen S., Gfeller D., Buth S.A., Michielin O., Leiman P.G., Heinis C.
ISSN
1439-7633 (Electronic)
ISSN-L
1439-4227
Publication state
Published
Issued date
2013
Peer-reviewed
Oui
Volume
14
Number
11
Pages
1316-1322
Language
english
Abstract
Improving the binding affinity and/or stability of peptide ligands often requires testing of large numbers of variants to identify beneficial mutations. Herein we propose a type of mutation that promises a high success rate. In a bicyclic peptide inhibitor of the cancer-related protease urokinase-type plasminogen activator (uPA), we observed a glycine residue that has a positive ϕ dihedral angle when bound to the target. We hypothesized that replacing it with a D-amino acid, which favors positive ϕ angles, could enhance the binding affinity and/or proteolytic resistance. Mutation of this specific glycine to D-serine in the bicyclic peptide indeed improved inhibitory activity (1.75-fold) and stability (fourfold). X-ray-structure analysis of the inhibitors in complex with uPA showed that the peptide backbone conformation was conserved. Analysis of known cyclic peptide ligands showed that glycine is one of the most frequent amino acids, and that glycines with positive ϕ angles are found in many protein-bound peptides. These results suggest that the glycine-to-D-amino acid mutagenesis strategy could be broadly applied.
Keywords
Amino Acids/metabolism, Binding Sites, Catalytic Domain, Crystallography, X-Ray, Databases, Protein, Enzyme Inhibitors/chemical synthesis, Enzyme Inhibitors/chemistry, Glycine/metabolism, Humans, Kinetics, Ligands, Mutagenesis, Site-Directed, Peptide Library, Peptides/chemistry, Peptides/genetics, Protein Binding, Protein Stability, Proteolysis, Substrate Specificity, Urokinase-Type Plasminogen Activator/antagonists & inhibitors, Urokinase-Type Plasminogen Activator/metabolism
Pubmed
Web of science
Create date
15/12/2014 14:20
Last modification date
20/08/2019 14:21
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