Poly-histidine grafting leading to fishbone-like architecturesElectronic supplementary information (ESI) available: ESI mass spectrum of Ac-His-6-MBHA-1d material; 1H and 13C NMR of compounds 1a-e, 2a-d, 3a-c, 5, 6a,b, and 8; photoluminescence of the polymeric materials obtained by exciting at different wavelengths. CCDC 1504772. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ra00315g

A small series of Morita-Baylis-Hillman adduct (MBHA) derivatives was synthesized and made to react with imidazole, N -acetylhistidine, and N -acetylhexahistidine as models of poly-histidine derivatives. Intriguingly, the reaction of MBHA derivatives 1a and b with imidazole in acetonitrile-phosphate...

Full description

Saved in:
Bibliographic Details
Main Authors Razzano, Vincenzo, Paolino, Marco, Reale, Annalisa, Giuliani, Germano, Donati, Alessandro, Giorgi, Gianluca, Artusi, Roberto, Caselli, Gianfranco, Visintin, Michela, Makovec, Francesco, Battiato, Salvatore, Samperi, Filippo, Villafiorita-Monteleone, Francesca, Botta, Chiara, Cappelli, Andrea
Format Journal Article
LanguageEnglish
Published 26.02.2018
Online AccessGet full text

Cover

Loading…
More Information
Summary:A small series of Morita-Baylis-Hillman adduct (MBHA) derivatives was synthesized and made to react with imidazole, N -acetylhistidine, and N -acetylhexahistidine as models of poly-histidine derivatives. Intriguingly, the reaction of MBHA derivatives 1a and b with imidazole in acetonitrile-phosphate buffered saline (PBS) gave the imidazolium salt biadducts 3a and b as the main reaction products. These results were confirmed by experiments performed with N -acetylhistidine and 1b and suggested the possible occurrence of these structures in the products of poly-histidine labeling with MBHA derivatives 1a and b . These compounds were then transformed into the corresponding water-soluble derivatives 1c-e by introducing oligo(ethylene glycol) chains and their reactivity was evaluated in preliminary experiments with imidazole and then with N -acetylhexahistidine in PBS. The structure of polymeric materials Ac-His-6-MBHA-1d and Ac-His-6-MBHA-1e obtained using ten-fold excesses of compounds 1d and e was investigated using mass spectrometry, NMR spectroscopy, and photophysical studies, which suggested the presence of biadduct residues in both polymeric materials. These results provide the basis for the preparation of fishbone-like polymer brushes, the characterization of their properties, and the exploration of their potential applications in different fields of science such as in vivo fluorogenic labeling, fluorescence microscopy, protein PEGylation, up to the production of smart materials and biosensors. A small series of Morita-Baylis-Hillman derivatives was synthesized and made to react with N -acetylhexahistidine to give polymeric materials characterized by the presence of biadduct residues.
Bibliography:Ac-His-6-MBHA-1d
13
b
C NMR of compounds
Electronic supplementary information (ESI) available: ESI mass spectrum of
6a
,
1
photoluminescence of the polymeric materials obtained by exciting at different wavelengths. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
10.1039/c8ra00315g
material
5
1504772
and
8
H and
3a-c
2a-d
1a-e
ISSN:2046-2069
DOI:10.1039/c8ra00315g