We report here on the efficient and straightforward synthesis of a series of modular and functional PBA-BODIPY dyes 1–4. They are an outstanding example of the efficient merge of the versatility of the 3,5-dichloro-BODIPY derivatives and the receptor-like ability of the PBA moiety. The potential bioanalytical applicability of these tools was assessed by measuring the binding to glycan chains of antibodies by a Quartz Crystal Microbalance (QCM).
A straightforward synthesis of phenyl boronic acid (PBA) containing BODIPY dyes: new functional and modular fluorescent tools for the tethering of the glycan domain of antibodies / Giacomazzo, Gina Elena; Palladino, Pasquale; Gellini, Cristina; Salerno, Gianluca; Baldoneschi, Veronica; Feis, Alessandro; Scarano, Simona; Minunni, Maria; Richichi, Barbara. - In: RSC ADVANCES. - ISSN 2046-2069. - ELETTRONICO. - 9:(2019), pp. 30773.30773-30773.30777. [10.1039/C9RA07608E]
A straightforward synthesis of phenyl boronic acid (PBA) containing BODIPY dyes: new functional and modular fluorescent tools for the tethering of the glycan domain of antibodies
GIACOMAZZO, GINA ELENA;Palladino, Pasquale;Gellini, Cristina;Salerno, Gianluca;Baldoneschi, Veronica;Feis, Alessandro;Scarano, Simona;Minunni, Maria;Richichi, Barbara
2019
Abstract
We report here on the efficient and straightforward synthesis of a series of modular and functional PBA-BODIPY dyes 1–4. They are an outstanding example of the efficient merge of the versatility of the 3,5-dichloro-BODIPY derivatives and the receptor-like ability of the PBA moiety. The potential bioanalytical applicability of these tools was assessed by measuring the binding to glycan chains of antibodies by a Quartz Crystal Microbalance (QCM).File | Dimensione | Formato | |
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