Proteomics

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


ABSTRACT: Here, we profiled sulfur(VI) fluorides (SVI-F) as reactive functionalities that can modify multiple residues including Lys, Tyr, His and Ser, thus offering utility for targeting almost any protein. These studies provided an in-depth understanding of SVI-F functionalities, including hydrolytic stability, protein reactivity and utility in chemoproteomics

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Aini Vuorinen  

LAB HEAD: Jacob Bush

PROVIDER: PXD037048 | Pride | 2024-03-18

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
ELN17365_10_40per_DIA_88min.raw Raw
ELN17365_11_40per_DIA_88min.raw Raw
ELN17365_12_40per_DIA_88min.raw Raw
ELN17365_13_40per_DIA_88min.raw Raw
ELN17365_14_40per_DIA_88min.raw Raw
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Profiling Sulfur(VI) Fluorides as Reactive Functionalities for Chemical Biology Tools and Expansion of the Ligandable Proteome.

Gilbert Katharine E KE   Vuorinen Aini A   Aatkar Arron A   Pogány Peter P   Pettinger Jonathan J   Grant Emma K EK   Kirkpatrick Joanna M JM   Rittinger Katrin K   House David D   Burley Glenn A GA   Bush Jacob T JT  

ACS chemical biology 20230117 2


Here, we report a comprehensive profiling of sulfur(VI) fluorides (S<sup>VI</sup>-Fs) as reactive groups for chemical biology applications. S<sup>VI</sup>-Fs are reactive functionalities that modify lysine, tyrosine, histidine, and serine sidechains. A panel of S<sup>VI</sup>-Fs were studied with respect to hydrolytic stability and reactivity with nucleophilic amino acid sidechains. The use of S<sup>VI</sup>-Fs to covalently modify carbonic anhydrase II (CAII) and a range of kinases was then inv  ...[more]

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