硫
化学
亲核细胞
连接器
硫化物
氮气
硫醇
刺激
高分子化学
组合化学
光化学
生物化学
有机化学
催化作用
盐(化学)
神经科学
计算机科学
生物
操作系统
作者
Fateme Zare,Patrick Laplante,Andrea A. Greschner,Jean‐François Cailhier,Marc A. Gauthier
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-08-21
卷期号:25 (9): 6017-6025
被引量:2
标识
DOI:10.1021/acs.biomac.4c00683
摘要
Chemical linkages that respond to biological stimuli are important for many pharmaceutical and biotechnological applications, making it relevant to explore new variants with different responsivity profiles. This work explores the responsiveness of a TAT peptide-based sulfonium vinyl sulfide probe that responds to nucleophilic thiols, radical thiol species (RTS), and reactive nitrogen species (RNS). Under model conditions, response to nucleophilic thiols was very slow (hours/days), though fast with down to molar equivalents of either RTS or RNS (minutes). These reactions led to the traceless release of a methionine-containing peptide in the first two cases and to a hydroxy nitration adduct in the third case. Despite the sensitive nature of the probe, it remained stable for at least ∼2 h in the presence of cells during TAT-mediated trafficking, even under pro-inflammatory stimulation. The thiol-responsiveness is intermediate to that observed for disulfide linkers and conventional cysteine-maleimide linkers, presenting opportunities for biotechnological applications.
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