Articolo in rivista, 2020, ENG, 10.3389/fchem.2020.616961
Gaeta, Massimiliano; Randazzo, Rosalba; Villari, Valentina; Micali, Norberto; Pezzella, Alessandro; Purrello, Roberto; d'Ischia, Marco; D'Urso, Alessandro
Univ Catania; CNR-IPCF; Univ Naples Federico II
Chiral porphyrin hetero-aggregates, produced from meso-tetrakis(4-N-methylpyridyl) porphyrin H(2)T4 and copper(II) meso-tetrakis(4-sulfonatophenyl)porphyrin CuTPPS by an imprinting effect in the presence of L-3,4-dihydroxyphenylalanine (L-DOPA), are shown herein to serve as templates for the generation of chiral structures during the oxidative conversion of the amino acid to melanin. This remarkable phenomenon is suggested to involve the initial role of L-DOPA and related chiral intermediates like dopachrome as templates for the production of chiral porphyrin aggregates. When the entire chiral pool from DOPA is lost, chiral porphyrin hetero-aggregate would elicit axially chiral oligomer formation from 5,6-dihydroxyindole intermediates in the later stages of melanin synthesis. These results, if corroborated by further studies, may open unprecedented perspectives for efficient strategies of asymmetric melanin synthesis with potential biological and technological applications.
Frontiers in Chemistry 8
eumelanin, DOPA, porphyrin, supramolecular aggregates, circular dichroism
Villari Valentina, Micali Norberto Liborio
ID: 446618
Year: 2020
Type: Articolo in rivista
Creation: 2021-03-01 17:56:24.000
Last update: 2021-03-07 19:53:27.000
CNR authors
CNR institutes
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:446618
DOI: 10.3389/fchem.2020.616961
ISI Web of Science (WOS): 000604296300001
Scopus: 2-s2.0-85098795345