Phage Display Selection of Ligand Residues Important for Src Homology 3 Domain Binding Specificity

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 92; no. 24; pp. 10909 - 10913
• Main Authors: Rickles, Richard J., Botfield, Martyn C., Zhou, Xiao-Mai, Henry, Pamela A., Brugge, Joan S.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences of the United States of America 21.11.1995; National Acad Sciences; National Academy of Sciences
• Subjects: Amino Acid Sequence; Amino acids; Bacteriophage M13; Bacteriophages; Binding sites; Biochemistry; Consensus sequence; Fluorescence; Gene Library; Libraries; Ligands; Molecular Sequence Data; Peptides - chemistry; phage M13; Protein Binding; Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Signal Transduction; src Homology Domains; Structure-Activity Relationship
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.92.24.10909

The Src homology 3 (SH3) domain is a 50-aa modular unit present in many cellular proteins involved in intracellular signal transduction. It functions to direct protein-protein interactions through the recognition of proline-rich motifs on associated proteins. SH3 domains are important regulatory elements that have been demonstrated to specify distinct regulatory pathways important for cell growth, migration, differentiation, and responses to the external milieu. By the use of synthetic peptides, ligands have been shown to consist of a minimum core sequence and to bind to SH3 domains in one of two pseudosymmetrical orientations, class I and class II. The class I sites have the consensus sequence ZP(L/P)PPΨP whereas the class II consensus is PPΨPPZ (where Ψ is a hydrophobic residue and Z is a SH3 domain-specific residue). We previously showed by M13 phage display that the Src, Fyn, Lyn, and phosphatidylinositol 3-kinase (PI3K) SH3 domains preferred the same class I-type core binding sequence, RPLPPΨP. These results failed to explain the specificity for cellular proteins displayed by SH3 domains in cells. In the current study, class I and class II core ligand sequences were displayed on the surface of bacteriophage M13 with five random residues placed either N- or C-terminal of core ligand residues. These libraries were screened for binding to the Src, Fyn, Lyn, Yes, and PI3K SH3 domains. By this approach, additional ligand residue preferences were identified that can increase the affinity of SH3 peptide ligands at least 20-fold compared with core peptides. The amino acids selected in the flanking sequences were similar for Src, Fyn, and Yes SH3 domains; however, Lyn and PI3K SH3 domains showed distinct binding specificities. These results indicate that residues that flank the core binding sequences shared by many SH3 domains are important determinants of SH3 binding affinity and selectivity.