Discovery of high-affinity peptide binders to BLyS by phage display

J Mol Recognit. 2005 Jan-Feb;18(1):94-102. doi: 10.1002/jmr.722.

Abstract

B lymphocyte stimulator (BLyS) is a tumor necrosis factor (TNF) family member and a key regulator of B cell responses. We employed a phage display-based approach to identify peptides that bind BLyS with high selectivity and affinity. Sequence analysis of first-generation BLyS-binding peptides revealed two dominant peptide motifs, including one containing a conserved DxLT sequence. Selected linear peptides with this motif were found to bind BLyS with K(D) values of 1-3 microM. In order to improve the binding affinity for BLyS, consensus residues flanking the DxLT sequence were seeded into a second-generation, BLyS affinity maturation library (BAML). BAML phage were subjected to stringent binding competition conditions to select for isolates expressing high-affinity peptide ligands for BLyS. Post-selection analysis of BAML peptide sequences resulted in the identification of a core decapeptide motif (WYDPLTKLWL). Peptides containing this core motif exhibited K(D) values as low as 26 nM, approximately 100-fold lower than that of first-generation peptides. A fluorescence anisotropy assay was developed to monitor the protein-protein interaction between BLyS labeled with a ruthenium chelate, and TACI-Fc, a soluble form of a BLyS receptor. Using this assay it was found that a BAML peptide disrupts this high-affinity protein-protein interaction. This demonstrates the potential of short peptides for disruption of high affinity cytokine-receptor interactions.

MeSH terms

  • Amino Acid Motifs
  • B-Cell Activating Factor
  • Biological Assay
  • Conserved Sequence
  • Disulfides / chemistry
  • Fluorescence Polarization
  • Humans
  • Membrane Proteins / antagonists & inhibitors*
  • Membrane Proteins / chemistry*
  • Membrane Proteins / metabolism
  • Membrane Proteins / physiology
  • Peptide Library*
  • Peptides / chemistry*
  • Peptides / isolation & purification*
  • Peptides / metabolism
  • Protein Interaction Mapping / methods
  • Receptors, Tumor Necrosis Factor / chemistry*
  • Receptors, Tumor Necrosis Factor / physiology
  • Ruthenium / chemistry
  • Transmembrane Activator and CAML Interactor Protein
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors*
  • Tumor Necrosis Factor-alpha / chemistry*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • B-Cell Activating Factor
  • Disulfides
  • Membrane Proteins
  • Peptide Library
  • Peptides
  • Receptors, Tumor Necrosis Factor
  • TNFRSF13B protein, human
  • TNFSF13B protein, human
  • Transmembrane Activator and CAML Interactor Protein
  • Tumor Necrosis Factor-alpha
  • Ruthenium