Minimalistic peptidic scaffolds harbouring an artificial carbene-containing amino acid modulate reductase activity.

Chem Commun (Camb)

Department of Chemistry, Biochemistry & Pharmaceutical Sciences, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.

Published: September 2021

Inspired by the boom of new artificial metalloenzymes, we developed an Fmoc-protected histidinium salt (Hum) as N-heterocyclic carbene precursor. Hum was placed solid-phase peptide synthesis into short 7-mer peptides. Upon iridation, the metallo-peptidic construct displayed activity in catalytic hydrogenation that outperforms small molecule analogues and which is dependent on the peptide sequence, a typical feature of metalloenzymes.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427656PMC
http://dx.doi.org/10.1039/d1cc03158aDOI Listing

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