Birolo, L., Sacchi, S., Smaldone, G., Molla, G., Leo, G., Caldinelli, L., Pirone, L., Eliometri, P., Di Gaetano, S., Orefice, I., Pedone, E., Pucci, P., Pollegioni, L.
Regulating levels of the neuromodulator d-serine in human brain: structural insight into pLG72 and d-amino acid oxidase interaction
(2016) FEBS Journal, pp. 3353-3370.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987974333&partnerID=40&md5=e4d80b1adf1d88a06d142c226e347d5c
DOI: 10.1111/febs.13809
AFFILIATIONS: Dipartimento di Scienze Chimiche, Università degli Studi di Napoli Federico II, Napoli, Italy;
Dipartimento di Biotecnologie e Scienze della Vita, Università degli studi dell'Insubria, Varese, Italy;
Centro Interuniversitario di Ricerca in Biotecnologie Proteiche “The Protein Factory”, Politecnico di Milano and Università degli studi dell'Insubria, Milano, Italy;
IRCCS SDN, Napoli, Italy;
Italian Research National Council, Institute of Biostructures and Bioimaging, Napoli, Italy
ABSTRACT: The human flavoenzyme d-amino acid oxidase (hDAAO) degrades the NMDA-receptor modulator d-serine in the brain. Although hDAAO has been extensively characterized, little is known about its main modulator pLG72, a small protein encoded by the primate-specific gene G72 that has been associated with schizophrenia susceptibility. pLG72 interacts with neosynthesized hDAAO, promoting its inactivation and degradation. In this work, we used low-resolution techniques to characterize the surface topology of the hDAAO–pLG72 complex. By using limited proteolysis coupled to mass spectrometry, we could map the exposed regions in the two proteins after complex formation and highlighted an increased sensitivity to proteolysis of hDAAO in complex with pLG72. Cross-linking experiments by using bis(sulfosuccinimidyl)suberate identified the single covalent bond between T182 in hDAAO and K62 in pLG72. In order to validate the designed mode of interaction, three pLG72 variants incrementally truncated at the C terminus, in addition to a form lacking the 71 N-terminal residues, were produced. All variants were dimeric, folded, and interacted with hDAAO. The strongest decrease in affinity for hDAAO (as well as for the hydrophobic drug chlorpromazine) was apparent for the N-terminally deleted pLG7272–153 form, which lacked K62. On the other hand, eliminating the disordered C-terminal tail yielded a more stable pLG72 protein, improved the binding to hDAAO, although giving lower enzyme inhibition. Elucidation of the mode of hDAAO–pLG72 interaction now makes it possible to design novel molecules that, by targeting the protein complex, can be therapeutically advantageous for diseases related to impairment in d-serine metabolism. © 2016 Federation of European Biochemical Societies
CORRESPONDENCE ADDRESS: Pollegioni, L.; Dipartimento di Biotecnologie e Scienze della Vita, Università degli studi dell'InsubriaItaly; email: loredano.pollegioni@uninsubria.it
DOCUMENT TYPE: Article
