Optimization of the Azobenzene Scaffold for Reductive Cleavage by Dithionite; Development of an Azobenzene Cleavable Linker for Proteomic Applications
✍ Scribed by Geoffray Leriche; Ghyslain Budin; Laurent Brino; Alain Wagner
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 250 KB
- Volume
- 2010
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Abstract
In this paper we conducted an extensive reactivity study to determine the key structural features that favour the dithionite‐triggered reductive cleavage of the azo–arene group. Our stepwise investigation allowed identification of a highly reactive azo–arene structure 25 bearing a carboxylic acid at the ortho position of the electron‐poor arene and an ortho‐O‐alkyl‐resorcinol as the electron‐rich arene. Based on this 2‐(2′‐alkoxy‐4′‐hydroxyphenylazo)benzoic acid (HAZA) scaffold, the orthogonally protected difunctional azo–arene cleavable linker 26 was designed and synthesized. Selective linker deprotection and derivatization was performed by introducing an alkyne reactive group and a biotin affinity tag. This optimized azo–arene cleavable linker led to a total cleavage in less than 10 s with only 1 mM dithionite. Similar results were obtained in biological media.