Issue 53, 2019

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

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).

Graphical abstract: 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

Supplementary files

Article information

Article type
Paper
Submitted
31 Jul 2019
Accepted
24 Sep 2019
First published
30 Sep 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 30773-30777

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

G. E. Giacomazzo, P. Palladino, C. Gellini, G. Salerno, V. Baldoneschi, A. Feis, S. Scarano, M. Minunni and B. Richichi, RSC Adv., 2019, 9, 30773 DOI: 10.1039/C9RA07608E

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