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Profiling Sulfur(VI) Fluorides as Reactive Functionalities for Chemical Biology Tools and Expansion of the Ligandable Proteome.

Katharine E GilbertAini VuorinenArron AatkarPeter PogányJonathan PettingerEmma K GrantJoanna M KirkpatrickKatrin RittingerDavid HouseGlenn A BurleyJacob T Bush
Published in: ACS chemical biology (2023)
Here, we report a comprehensive profiling of sulfur(VI) fluorides (S VI -Fs) as reactive groups for chemical biology applications. S VI -Fs are reactive functionalities that modify lysine, tyrosine, histidine, and serine sidechains. A panel of S VI -Fs were studied with respect to hydrolytic stability and reactivity with nucleophilic amino acid sidechains. The use of S VI -Fs to covalently modify carbonic anhydrase II (CAII) and a range of kinases was then investigated. Finally, the S VI -F panel was used in live cell chemoproteomic workflows, identifying novel protein targets based on the type of S VI -F used. This work highlights how S VI -F reactivity can be used as a tool to expand the liganded proteome.
Keyphrases
  • amino acid
  • single cell
  • small molecule
  • high resolution
  • binding protein