Deeper insight into protease-sensitive "covalent-assembly" fluorescent probes for practical biosensing applications. Issue 39 (27th September 2019)
- Record Type:
- Journal Article
- Title:
- Deeper insight into protease-sensitive "covalent-assembly" fluorescent probes for practical biosensing applications. Issue 39 (27th September 2019)
- Main Title:
- Deeper insight into protease-sensitive "covalent-assembly" fluorescent probes for practical biosensing applications
- Authors:
- Renault, Kévin
Debieu, Sylvain
Richard, Jean-Alexandre
Romieu, Anthony - Abstract:
- Abstract : The properties and versatility of protease-responsive "covalent-assembly" fluorescent probes are optimised in an effective and rational manner, through structural diversification of their Michael acceptor moiety. Abstract : We report a rational and systematic study devoted to the structural optimisation of a novel class of protease-sensitive fluorescent probes that we recently reported (S. Debieu and A. Romieu, Org. Biomol. Chem., 2017, 15, 2575–2584), based on the "covalent-assembly" strategy and using the targeted enzyme penicillin G acylase as a model protease to build a fluorescent pyronin dye by triggering a biocompatible domino cyclisation–aromatisation reaction. The aim is to identify ad hoc probe candidate(s) that might combine fast/reliable fluorogenic "turn-on" response, full stability in complex biological media and ability to release a second molecule of interest (drug or second fluorescent reporter), for applications in disease diagnosis and therapy. We base our strategy on screening a set of active methylene compounds (C-nucleophiles) to convert the parent probe to various pyronin caged precursors bearing Michael acceptor moieties of differing reactivities. In vitro stability and fluorescent enzymatic assays combined with HPLC-fluorescence analyses provide data useful for defining the most appropriate structural features for these fluorogenic scaffolds depending on the specifications inherent to biological application (from biosensing toAbstract : The properties and versatility of protease-responsive "covalent-assembly" fluorescent probes are optimised in an effective and rational manner, through structural diversification of their Michael acceptor moiety. Abstract : We report a rational and systematic study devoted to the structural optimisation of a novel class of protease-sensitive fluorescent probes that we recently reported (S. Debieu and A. Romieu, Org. Biomol. Chem., 2017, 15, 2575–2584), based on the "covalent-assembly" strategy and using the targeted enzyme penicillin G acylase as a model protease to build a fluorescent pyronin dye by triggering a biocompatible domino cyclisation–aromatisation reaction. The aim is to identify ad hoc probe candidate(s) that might combine fast/reliable fluorogenic "turn-on" response, full stability in complex biological media and ability to release a second molecule of interest (drug or second fluorescent reporter), for applications in disease diagnosis and therapy. We base our strategy on screening a set of active methylene compounds (C-nucleophiles) to convert the parent probe to various pyronin caged precursors bearing Michael acceptor moieties of differing reactivities. In vitro stability and fluorescent enzymatic assays combined with HPLC-fluorescence analyses provide data useful for defining the most appropriate structural features for these fluorogenic scaffolds depending on the specifications inherent to biological application (from biosensing to theranostics) for which they will be used. … (more)
- Is Part Of:
- Organic & biomolecular chemistry. Volume 17:Issue 39(2019)
- Journal:
- Organic & biomolecular chemistry
- Issue:
- Volume 17:Issue 39(2019)
- Issue Display:
- Volume 17, Issue 39 (2019)
- Year:
- 2019
- Volume:
- 17
- Issue:
- 39
- Issue Sort Value:
- 2019-0017-0039-0000
- Page Start:
- 8918
- Page End:
- 8932
- Publication Date:
- 2019-09-27
- Subjects:
- Chemistry, Organic -- Periodicals
Bioorganic chemistry -- Periodicals
Chemistry, Physical organic -- Periodicals
547 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ob#!recentarticles&all ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ob01773a ↗
- Languages:
- English
- ISSNs:
- 1477-0520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6286.350000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12027.xml