Easy Production of "Difficult Peptides" Using Cell-Free Protein Synthesis and a New Methionine Analogue as a Latent Peptide Cleavage Site.

Autor: Fankhauser D; Research School of Chemistry, Australian National University, 137 Sullivans Creek Road, Acton, ACT 2601, Australia., Alissandratos A; Research School of Chemistry, Australian National University, 137 Sullivans Creek Road, Acton, ACT 2601, Australia., Liutkus M; Research School of Chemistry, Australian National University, 137 Sullivans Creek Road, Acton, ACT 2601, Australia., Easton CJ; Research School of Chemistry, Australian National University, 137 Sullivans Creek Road, Acton, ACT 2601, Australia.
Jazyk: angličtina
Zdroj: Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2021 Dec 09; Vol. 27 (69), pp. 17487-17494. Date of Electronic Publication: 2021 Oct 29.
DOI: 10.1002/chem.202103161
Abstrakt: Aliphatic γ-chloro-α-amino acids incorporated in place of their canonical analogues through cell-free protein synthesis act as heat-labile linkers, offering a useful strategy for the straightforward production of target peptides as fusion proteins, from which the targets are readily released. Until now, the natural abundance of aliphatic amino acids in peptides has limited the scope of the method, as it leads to undesired cleavage sites in synthesized products, but here the authors report the development of a new cleavable chloro amino acid that incorporates in place of the relatively rare amino acid methionine, thus greatly expanding the scope of producible targets. This new strategy is employed for simplified peptide synthesis with a methionine-free fusion partner, allowing single-site incorporation of the cleavable linker for clean release and easy purification of the target peptide. Its utility is demonstrated through the straightforward preparation of two peptides reported to be challenging targets and not accessible through standard solid-phase chemical methodologies, as well as analogues.
(© 2021 Wiley-VCH GmbH.)
Databáze: MEDLINE