@article{10272/21354,
year = {2021},
month = {6},
url = {https://hdl.handle.net/10272/21354},
abstract = {The selective photodeprotection of the NVoc-modified FGG tripeptide yields the transformation of its 1:1 receptor−ligand complex with cucurbit[8]uril into a homoternary FGG2@CB8 assembly. The resulting lightinduced dimerization of the model peptide provides a tool for the implementation of stimuli-responsive supramolecular chemistry in biologically relevant contexts.},
organization = {The work was supported by the Associate Laboratory for Green ChemistryLAQV (UIDB/50006/2020) and by the Applied Molecular Biosciences UnitUCIBIO (UIDB/ 04378/2020), both financed by FCT. FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013-PINFRA/22161/2016, cofinanced by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grants PTDC/QUICOL/32351/2017, PTDC/QUI-QFI/30951/2017, and CEECIND/00466/2017 (N.B.). U.P. thanks the Spanish Ministry of Science, Innovation, and Universities (CTQ2017-89832-P). We are grateful to Dr. J.P. Da Silva for the mass spectrometry data (equipment financed by CRESC Algarve 2020 and COMPETE 2020; project EMBRC.PT ALG-01-0145-FEDER022121).
Funding for open access charge: Universidad de Huelva / CBUA},
publisher = {American Chemical Society},
title = {Toward Light-Controlled Supramolecular Peptide Dimerization},
doi = {10.1021/acs.joc.1c00464},
author = {Fernandes, Rita J. and Remón Ruiz, Patricia and Moro, Artur J. and Seco, André and Ferreira, Ana S. D. and Pischel, Uwe and Basílio, Nuno},
}