Robo2 contains a cryptic binding site for neural EGFL-like (NELL) protein 1/2

• Published in: The Journal of biological chemistry Vol. 294; no. 12; pp. 4693 - 4703
• Main Authors: Yamamoto, Naoka, Kashiwagi, Manabu, Ishihara, Manami, Kojima, Takaaki, Maturana, Andrés D., Kuroda, Shun’ichi, Niimi, Tomoaki
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 22.03.2019; American Society for Biochemistry and Molecular Biology
• Subjects: Acids; Amino Acid Sequence; Amino Acid Substitution; Binding Sites; Calcium-Binding Proteins; cell surface receptor; Humans; Hydrogen-Ion Concentration; Mutation; Nerve Tissue Proteins - metabolism; protein conformation; protein domain; Protein Structure and Folding; protein-protein interaction; Proteolysis; Receptors, Immunologic - chemistry; Receptors, Immunologic - genetics; Receptors, Immunologic - metabolism; structural model; protein domain; protein conformation; protein-protein interaction; cell surface receptor; structural model
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.RA118.005819

The signaling pathways that are mediated by Slit ligands and their Roundabout (Robo) family of receptors play multifunctional roles in the development of the nervous system and other organs. A recent study identified neural epidermal growth factor–like (NEL)–like 2 (NELL2) as a novel ligand for Robo3. In this study, we carried out a comprehensive analysis of the interaction between NELL1 and the Robo family of receptors and demonstrated that Robo2 contains a cryptic binding site for both NELL1 and NELL2. NELL1/2 binds to the first fibronectin type III (FNIII) domain of Robo2 but not to intact Robo2. Mutation analysis revealed that several amino acids within the first FNIII domain are critical for NELL1 binding to Robo2 but not to Robo1. The Robo2 deletion mutants without the fourth immunoglobulin domain and single amino acid substitution mutants that can influence the architecture of the ectodomain facilitated binding to NELL1/2. Acidic conditions increased the binding affinity of Robo2 for NELL1. These results suggest that Robo2 functions as a receptor for NELL1/2, particularly under circumstances where Robo2 undergoes proteolytic digestion. If this is not the case, conformational changes of the ectodomain of Robo2 may unmask the binding site for NELL1/2.