NMR uncovers direct interaction between human NEDD4-1 and p34SEI−1

PTEN, an important tumor suppressor and a key regulator of the PI3K/AKT signaling pathway, is often deleted/mutated in different types of cancer. The E3 ubiquitin ligase NEDD4-1 catalyzes the polyubiquitination of PTEN, thereby acting as a negative regulator of PTEN. Stability of NEDD4-1, in turn, is tightly controlled by a 34 kDa oncoprotein, p34SEI−1 and it regulates PTEN degradation and activates PI3K/AKT pathway, resulting in cancer metastasis. p34SEI−1 affects not only the expression of NEDD4-1 during transcription and translation but also the subcellular localization of PTEN. This emphasizes the need to understand, at molecular level, the interaction between NEDD4-1 and p34SEI−1. A recent study showed that NEDD4-1 interacts with p34SEI−1 via its WWI domain. However, a detailed interaction for molecular level is yet unknown. We report that the WW1 domain of NEDD4-1 recognizes the SERTA domain containing the proline rich region (PRR motif) in p34SEI−1. TALOS analysis based on NMR data confirms three conserved β-sheets in NEDD4-1 WW1 and the central β-sheet of NEDD4-1 WW1 plays a role for protein stability by the backbone dynamics experiments. NMR titration data revealed the binding site for p34SEI−1 with NEDD4-1. Our data will provide insights into the molecular mechanism of NEDD4-1 and p34SEI−1 interaction, which will be directly used for drug design which inhibits the molecular interaction involved in different cancer signaling. •NEDD4-1 recognizes SERTA domain containing proline rich region of p34SEI−1.•TALOS analysis based on NMR data confirms three conserved β-sheets in NEDD4-1 WW1.•The central β-sheet of NEDD4-1 WW1 provides protein stability as indicated by the backbone dynamics data.•Residues of NEDD4-1 responsible for direct interaction with p34SEI−1 are identified by NMR titration experiments.•Our data will be of essence in designing inhibitors for NEDD4-1/p34SEI−1 interaction.