Glutathione-Responsive Fragmentation of Heteronorbornadiene-Based Thiovinyl Sulfones in Glioma Cells

We report the synthesis and fluorescent properties of dansylated heteronorbornadienes (HNDs) featuring a thiovinyl sulfone moiety as a thiol-reactive trigger. These systems undergo thiol addition which promotes fragmentation via a thioketal intermediate, leading to the release of fluorescent heterocycles (furan or pyrrole) and ketene S,S-acetals. Distinct fluorescence signatures enable real-time monitoring of the fragmentation process. We also report cellular studies to demonstrate that HND-thiovinyl sulfones are membrane-permeable and undergo glutathione (GSH)-mediated activation in glioma cells, resulting in intracellular release of fluorescent products. These findings establish HND-based architectures as promising platforms for the design of cleavable linkers in controlled release applications, particularly in targeted drug delivery and theranostics where stimuli-responsive behavior is essential.

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Publication Details

Journal
Bioconjugate Chemistry
Published
2026-04-28
DOI
https://doi.org/10.1021/acs.bioconjchem.5c00581
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Glutathione-Responsive Fragmentation of Heteronorbornadiene-Based Thiovinyl Sulfones in Glioma Cells

Gonçalo J. L. Bernardes, Enrique Gil de Montes, Yanira Méndez, Ana T. Carmona et al.
Bioconjugate Chemistry
Click Chemistry and Applications
article

Glutathione-Responsive Fragmentation of Heteronorbornadiene-Based Thiovinyl Sulfones in Glioma Cells

Gonçalo J. L. Bernardes, Enrique Gil de Montes, Yanira Méndez, Ana T. Carmona, Inga Černauskienė, Antonio J. Moreno-Vargas, Marina Carranza
article en

Abstract

We report the synthesis and fluorescent properties of dansylated heteronorbornadienes (HNDs) featuring a thiovinyl sulfone moiety as a thiol-reactive trigger. These systems undergo thiol addition which promotes fragmentation via a thioketal intermediate, leading to the release of fluorescent heterocycles (furan or pyrrole) and ketene S,S-acetals. Distinct fluorescence signatures enable real-time monitoring of the fragmentation process. We also report cellular studies to demonstrate that HND-thiovinyl sulfones are membrane-permeable and undergo glutathione (GSH)-mediated activation in glioma cells, resulting in intracellular release of fluorescent products. These findings establish HND-based architectures as promising platforms for the design of cleavable linkers in controlled release applications, particularly in targeted drug delivery and theranostics where stimuli-responsive behavior is essential.

Bioconjugate Chemistry
University of Cambridge (GB), Spanish National Cancer Research Centre (ES), Universidad de Sevilla (ES)
Ministerio de Ciencia, Innovación y Universidades
Good health and well-being
Openalex Percentile: Top 12%
Click Chemistry and Applications
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