| Title: |
A novel tyrosine hyperoxidation enables selective peptide cleavage |
| Authors: |
Zhang, S; De Leon Rodriguez, LM; Li, FF; Huang, R; Leung, IKH; Harris, PWR; Brimble, MA |
| Publisher Information: |
ROYAL SOC CHEMISTRY |
| Publication Year: |
2022 |
| Collection: |
The University of Melbourne: Digital Repository |
| Description: |
A novel tyrosine hyperoxidation enabling selective peptide cleavage is reported. The scission of the N-terminal amide bond of tyrosine was achieved with Dess-Martin periodinane under mild conditions, generating a C-terminal peptide fragment bearing the unprecedented hyperoxidized tyrosine motif, 4,5,6,7-tetraoxo-1H-indole-2-carboxamide, along with an intact N-terminal peptide fragment. This reaction proceeds with high site-selectivity for tyrosine and exhibits broad substrate scope for various peptides, including those containing post-translational modifications. More importantly, this oxidative cleavage was successfully applied to enable sequencing of three naturally occurring cyclic peptides, including one depsipeptide and one lipopeptide. The linearized peptides generated from the cleavage reaction significantly simplify cyclic peptide sequencing by MS/MS, thus providing a robust tool to facilitate rapid sequence determination of diverse cyclic peptides containing tyrosine. Furthermore, the highly electrophilic nature of the hyperoxidized tyrosine unit disclosed in this work renders it an important electrophilic target for the selective bioconjugation or synthetic manipulation of peptides containing this unit. |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| ISSN: |
2041-6520 |
| Relation: |
pii: d1sc06216f; https://hdl.handle.net/11343/302454 |
| Availability: |
https://hdl.handle.net/11343/302454 |
| Rights: |
https://creativecommons.org/licenses/by-nc/4.0 ; CC BY-NC |
| Accession Number: |
edsbas.722684E7 |
| Database: |
BASE |