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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).

SUBMITTER: Giacomazzo GE 

PROVIDER: S-EPMC9072199 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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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 GE   Palladino Pasquale P   Gellini Cristina C   Salerno Gianluca G   Baldoneschi Veronica V   Feis Alessandro A   Scarano Simona S   Minunni Maria M   Richichi Barbara B  

RSC advances 20190930 53


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). ...[more]

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