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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]·(...

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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
Descripción
Sumario: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.