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DNAzymes for amine and peptide lysine acylation.

Authors :
Yao T
Przybyla JJ
Yeh P
Woodard AM
Nilsson HJ
Brandsen BM
Silverman SK
Source :
Organic & biomolecular chemistry [Org Biomol Chem] 2021 Jan 06; Vol. 19 (1), pp. 171-181.
Publication Year :
2021

Abstract

DNAzymes were previously identified by in vitro selection for a variety of chemical reactions, including several biologically relevant peptide modifications. However, finding DNAzymes for peptide lysine acylation is a substantial challenge. By using suitably reactive aryl ester acyl donors as the electrophiles, here we used in vitro selection to identify DNAzymes that acylate amines, including lysine side chains of DNA-anchored peptides. Some of the DNAzymes can transfer a small glutaryl group to an amino group. These results expand the scope of DNAzyme catalysis and suggest the future broader applicability of DNAzymes for sequence-selective lysine acylation of peptide and protein substrates.

Details

Language :
English
ISSN :
1477-0539
Volume :
19
Issue :
1
Database :
MEDLINE
Journal :
Organic & biomolecular chemistry
Publication Type :
Academic Journal
Accession number :
33150349
Full Text :
https://doi.org/10.1039/d0ob02015j