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Synlett 2019; 30(19): 2123-2130
DOI: 10.1055/s-0039-1690711
DOI: 10.1055/s-0039-1690711
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Reprogramming Nonribosomal Peptide Synthesis by Surgical Mutation
This work was generously funded by the Swiss National Science Foundation and the ETH Zurich. D.A.H. is grateful for an ETH Zurich Postdoctoral Fellowship that was co-funded by the Marie Curie Actions program.Further Information
Publication History
Received: 20 August 2019
Accepted after revision: 25 September 2019
Publication Date:
28 October 2019 (online)
Abstract
Nonribosomal peptide synthetases produce highly modified bioactive peptides, many of which are used therapeutically. As such, they have been the target of intense protein engineering to enable biosynthetic access to peptide variants with improved drug properties or altered bioactivities. In this account, we describe our ongoing efforts to reprogram nonribosomal peptide synthesis by surgical mutation. In contrast to ribosomal biosynthesis, nonribosomal peptide synthesis has proven difficult to engineer, arguably due to a lack of suitable tools. To address this limitation, we have established a high-throughput assay that provides unprecedented control over the gatekeeper adenylation domains responsible for building block selection and incorporation. Expansion of this strategy to other building blocks and domains promises to make it a powerful evolutionary platform for tailoring assembly lines for custom synthesis of peptide therapeutics.
1. Nonribosomal Peptides
2. Reprogramming A Domains for Clickable Amino Acids
3 A High-Throughput A Domain Assay
4 Reprogramming A Domains for β-Amino Acids
5 Downstream Processing
6 Conclusions and Outlook
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