Thioredoxin reductase-triggered fluorogenic donor of hydrogen sulfide: a model study with a symmetrical organopolysulfide probe with turn-on near-infrared fluorescent emission
We describe herein the rational development of an organopolysulfide-based fluorogenic donor of hydrogen sulfide (H 2 S) DCI-PS , which can be activated by the antioxidant selenoenzyme thioredoxin reductase (TrxR) with concomitant release of the dicyanoisophorone-based near-infrared (NIR) fluorophore...
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Veröffentlicht in: | Journal of materials chemistry. B, Materials for biology and medicine Materials for biology and medicine, 2022-03, Vol.1 (13), p.2183-2193 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We describe herein the rational development of an organopolysulfide-based fluorogenic donor of hydrogen sulfide (H
2
S)
DCI-PS
, which can be activated by the antioxidant selenoenzyme thioredoxin reductase (TrxR) with concomitant release of the dicyanoisophorone-based near-infrared (NIR) fluorophore. Along with the polysulfide probe
DCI-PS
capable of releasing the NIR fluorophore and H
2
S, the corresponding disulfide-probe
DCI-DS
was also rationally designed and synthesized, which releases the fluorophore without donating H
2
S. Detailed spectroscopic and kinetic studies in an aqueous medium revealed significantly higher reactivity of the probes towards DTT (for TrxR activity) over the well-known cellular abundant biothiol GSH. Mechanistically, the nucleophilic attack at the disulfide/polysulfide linkage by the thiol/selenol group of the bio-analytes leads to the self-immolative cyclization process with the release of the turn-on fluorophore with/without H
2
S. Considering the overexpression of mammalian TrxR in cancer cells, the turn-on fluorogenic H
2
S donation process from the cellular non-toxic
DCI-PS
was validated in a representative breast cancer cell line (MDA-MB-231) for the sustained donation of H
2
S with concomitant release of the red-emitting NIR fluorophore. The TrxR-triggered fluorescence turn-on process in
DCI-PS
was further supported by the significant inhibition of the fluorogenic process in the presence of TrxR-selective small-molecule inhibitors and by the significant binding affinity predicted by the protein-ligand docking study. Results with the antioxidant enzyme-triggered intracellular sustained donation of H
2
S with concomitant fluorescence turn-on will certainly find wider biomedical applications in the near future, particularly in H
2
S-mediated therapeutics in disease states.
An antioxidant enzyme thioredoxin reductase (TrxR)-responsive fluorogenic donor of hydrogen sulfide with the concomitant release of a red-emitting NIR fluorophore is demonstrated. |
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ISSN: | 2050-750X 2050-7518 |
DOI: | 10.1039/d1tb02425f |