Profiling sulfur(VI) fluorides as reactive functionalities for chemical biology tools and expansion of the ligandable proteome
Gilbert, Katharine E. and Vuorinen, Aini and Aatkar, Arron and Pogány, Peter and Pettinger, Jonathan and Grant, Emma K. and Kirkpatrick, Joanna M. and Rittinger, Katrin and House, David and Burley, Glenn A. and Bush, Jacob T. (2023) Profiling sulfur(VI) fluorides as reactive functionalities for chemical biology tools and expansion of the ligandable proteome. ACS Chemical Biology, 18 (2). pp. 285-295. ISSN 1554-8937 (https://doi.org/10.1021/acschembio.2c00633)
Preview |
Text.
Filename: Gilbert_etal_ACSCB_2023_Profiling_sulfur_VI_fluorides_as_reactive_functionalities_for_chemical_biology_tools.pdf
Final Published Version License: Download (5MB)| Preview |
Abstract
Here, we report a comprehensive profiling study of sulfur(VI) fluorides (SVI-F) in the context of multiple chemical biology applications and illustrate that these motifs present an exciting opportunity to develop tools for a wide scope of protein targets. SVI-Fs are reactive functionalities that offer utility for targeting almost any protein, as they can modify multiple residues including Lys, Tyr, His and Ser. A panel of SVI-F functionalities were studied with respect to hydrolytic stability and reactivity with nucleophilic amino acids. Subsequently, the reactivity of SVI-Fs with CAII and kinase proteins was investigated, in the context of both fragment binders and optimized probes. Finally, the performance of the SVI-F panel in chemoproteomic workflows was analyzed. The studies provided an in-depth understanding of the hydrolytic stability, protein reactivity and chemoproteomic utility of SVI-F functionalities that are suitable for direct incorporation into chemical tools. Such insights offer a valuable guide for the prospective design of SVI-F-containing ligands for various chemical biology workflows and demonstrate the wide range of proteins that SVI-Fs can capture, thus highlighting the opportunity for SVI-Fs to expand the liganded proteome.
-
-
Item type: Article ID code: 83781 Dates: DateEvent17 February 2023Published17 January 2023Published Online5 January 2023AcceptedSubjects: Medicine > Biomedical engineering. Electronics. Instrumentation
Science > Chemistry > Physical and theoretical chemistryDepartment: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 20 Jan 2023 12:26 Last modified: 12 Dec 2024 14:13 URI: https://strathprints.strath.ac.uk/id/eprint/83781