Expanding the scope of copper artificial metalloenzymes: A potential fluorinase?
Biocatalysts for fluorination are rare, and thus of great interest for artificial enzyme design. Biohybrid catalysts including Cu-based DNAzymes and dinucleotide catalysts can catalyse enantioselective electrophilic fluorination of β-ketoesters. Here we report the investigation of Cu-based artificial metalloenzymes as catalysts for electrophilic fluorination reactions. A library of artificial copper proteins was prepared by bioconjugation of bidentate and tridentate nitrogen ligands to cysteine variants of the Sterol Carrier Protein 2 L (SCP-2 L) and subsequent addition of Cu(II) salts. The resulting copper proteins were screened for activity for the fluorination of β-ketoesters using Selectfluor. Under aqueous acidic conditions it was observed that the designed catalysts did not outcompete the uncatalysed background reaction. This work highlights that careful consideration of substrate reactivity and background reactions is needed when considering potential reactions for artificial metalloenzyme catalysis.
Authors
- Amanda G. Jarvis (ORCID: https://orcid.org/0000-0002-6414-0497)
- Isabeau Lüddecke
Institutions
- University of Edinburgh (GB)
Publication Details
- Journal
- Journal of Inorganic Biochemistry
- Published
- 2024-11-19
- DOI
- https://doi.org/10.1016/j.jinorgbio.2024.112777
- Citations
- 2
- Primary Topic
- Nanocluster Synthesis and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.23