A map of WW domain family interactions

• Published in: Proteomics (Weinheim) Vol. 4; no. 3; pp. 643 - 655
• Main Authors: Hu, Hai, Columbus, John, Zhang, Yi, Wu, Dongying, Lian, Lubing, Yang, Song, Goodwin, Jennifer, Luczak, Christine, Carter, Mark, Chen, Lin, James, Michael, Davis, Roger, Sudol, Marius, Rodwell, John, Herrero, Juan J.
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 01-03-2004; WILEY‐VCH Verlag; Wiley-VCH
• Subjects: Amino Acid Motifs; Amino Acid Sequence; Analytical, structural and metabolic biochemistry; Biological and medical sciences; Computational Biology; Cross-affinity binding matrixes; DNA Mutational Analysis; Enzyme-Linked Immunosorbent Assay; Fundamental and applied biological sciences. Psychology; Glutathione Transferase - metabolism; Humans; Ligands; Miscellaneous; Molecular Sequence Data; Peptides - chemistry; Proline - chemistry; Proline-rich peptides; Protein Binding; Protein domains; Protein networks; Protein Structure, Secondary; Protein Structure, Tertiary; Protein-to-protein interaction; Proteins; Signal Transduction; Software; Proteomics
• ISSN: 1615-9853; 1615-9861
• DOI: 10.1002/pmic.200300632

WW domains are protein modules that bind proline‐rich ligands. WW domain‐ligand complexes are of importance as they have been implicated in several human diseases such as muscular dystrophy, cancer, hypertension, Alzheimer's, and Huntington's diseases. We report the results of a protein array aimed at mapping all the human WW domain protein‐protein interactions. Our biochemical approach integrates parallel synthesis of peptides, protein expression, and high‐throughput screening methodology combined with tools of bioinformatics. The results suggest that the majority of the bioinformatically predicted WW peptide ligands and most WW domains are functional, and that only about 10% of the measured domain‐ligand interactions are positive. The analysis of the WW domain protein arrays also underscores the importance of the amino acid residues surrounding the WW ligand core motifs for specific binding to WW domains. In addition, the methodology presented here allows for the rapid elucidation of WW domain‐ligand interactions with multiple applications including prediction of exact WW ligand binding sites, which can be applied to the mapping of other protein signaling domain families. Such information can be applied to the generation of protein interaction networks and identification of potential drug targets. To our knowledge, this report describes the first protein‐protein interaction map of a domain in the human proteome.