Cargando…

Design and recognition of cucurbituril-secured platinum-bound oligopeptides

Platinum terpyridyl complexes, stacked on top of one another and secured as dimers with cucurbit[8]uril (CB[8]) in aqueous medium, were functionalized quantitatively and in situ with a pair of pentapeptides Phe-(Gly)(3)-Cys by grafting their cysteine residues to the Pt centers. The resulting CB[8]·(...

Descripción completa

Detalles Bibliográficos
Autores principales: Barbero, Héctor, Masson, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317623/
https://www.ncbi.nlm.nih.gov/pubmed/34349966
http://dx.doi.org/10.1039/d1sc02637b
_version_ 1783730102886989824
author Barbero, Héctor
Masson, Eric
author_facet Barbero, Héctor
Masson, Eric
author_sort Barbero, Héctor
collection PubMed
description Platinum terpyridyl complexes, stacked on top of one another and secured as dimers with cucurbit[8]uril (CB[8]) in aqueous medium, were functionalized quantitatively and in situ with a pair of pentapeptides Phe-(Gly)(3)-Cys by grafting their cysteine residues to the Pt centers. The resulting CB[8]·(Pt·peptide)(2) assemblies were used to target secondary hosts CB[7] and CB[8] via their pair of phenylalanine residues, again in situ. A series of well-defined architectures, including a supramolecular “pendant necklace” with hybrid head-to-head and head-to-tail arrangements inside CB[8], were obtained during the self-sorting process after combining only 3 or 4 simple building units.
format Online
Article
Text
id pubmed-8317623
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-83176232021-08-03 Design and recognition of cucurbituril-secured platinum-bound oligopeptides Barbero, Héctor Masson, Eric Chem Sci Chemistry Platinum terpyridyl complexes, stacked on top of one another and secured as dimers with cucurbit[8]uril (CB[8]) in aqueous medium, were functionalized quantitatively and in situ with a pair of pentapeptides Phe-(Gly)(3)-Cys by grafting their cysteine residues to the Pt centers. The resulting CB[8]·(Pt·peptide)(2) assemblies were used to target secondary hosts CB[7] and CB[8] via their pair of phenylalanine residues, again in situ. A series of well-defined architectures, including a supramolecular “pendant necklace” with hybrid head-to-head and head-to-tail arrangements inside CB[8], were obtained during the self-sorting process after combining only 3 or 4 simple building units. The Royal Society of Chemistry 2021-06-17 /pmc/articles/PMC8317623/ /pubmed/34349966 http://dx.doi.org/10.1039/d1sc02637b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Barbero, Héctor
Masson, Eric
Design and recognition of cucurbituril-secured platinum-bound oligopeptides
title Design and recognition of cucurbituril-secured platinum-bound oligopeptides
title_full Design and recognition of cucurbituril-secured platinum-bound oligopeptides
title_fullStr Design and recognition of cucurbituril-secured platinum-bound oligopeptides
title_full_unstemmed Design and recognition of cucurbituril-secured platinum-bound oligopeptides
title_short Design and recognition of cucurbituril-secured platinum-bound oligopeptides
title_sort design and recognition of cucurbituril-secured platinum-bound oligopeptides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317623/
https://www.ncbi.nlm.nih.gov/pubmed/34349966
http://dx.doi.org/10.1039/d1sc02637b
work_keys_str_mv AT barberohector designandrecognitionofcucurbiturilsecuredplatinumboundoligopeptides
AT massoneric designandrecognitionofcucurbiturilsecuredplatinumboundoligopeptides