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]·(...
Autores principales: | , |
---|---|
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 |