Articolo in rivista, 2020, ENG, 10.3389/fchem.2020.616961

En Route to a Chiral Melanin: The Dynamic "From-Imprinted-to-Template" Supramolecular Role of Porphyrin Hetero-Aggregates During the Oxidative Polymerization of L-DOPA

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

Keywords

eumelanin, DOPA, porphyrin, supramolecular aggregates, circular dichroism

CNR authors

Villari Valentina, Micali Norberto Liborio

CNR institutes

IPCF – Istituto per i processi chimico-fisici

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

External links

OAI-PMH: Dublin Core

OAI-PMH: Mods

OAI-PMH: RDF

DOI: 10.3389/fchem.2020.616961

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