Kern, Dóra and Kormos, Attila (2023) Self-Immobilizing Quinone Methides for the Fluorescent Sensing of Enzyme Activity. CHEMOSENSORS, 11 (3). No. 155. ISSN 2227-9040
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Abstract
Gaining insight into biological processes relies on sensitive analytical techniques. These often require labeling of biomolecules that help visualize them. Selective covalent labeling without preliminary modification of the biomolecules is an advantageous method. For example, this can be achieved by using probes that are capable of in situ quinone methide (QM) formation. The QM can be masked to give a stable precursor, and the highly reactive form is only generated upon activation by a specific trigger. The in situ formed QM then binds covalently to the nucleophilic side chains of either the target protein or a protein in close proximity. Using fluorogenic probes further improves this method by reducing non-specific background signals, thus improving signal-to-noise ratios. In this review we summarize the development of quinone methide-based probes from mechanism-based inactivation to red-emitting, fluorogenic activity probes, focusing on enzyme-triggered activation.
Item Type: | Article |
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Uncontrolled Keywords: | quinone methides; fluorescence; activity probes; fluorogenic probes; self-immobilization |
Subjects: | Q Science / természettudomány > QD Chemistry / kémia Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia |
Depositing User: | Attila Kormos |
Date Deposited: | 21 Sep 2023 07:17 |
Last Modified: | 21 Sep 2023 07:17 |
URI: | http://real.mtak.hu/id/eprint/174261 |
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