Universal peptide synthesis via solid-phase methods fused with chemputation
Since the advent of automated solid-phase peptide synthesis (SPPS), many commercial platforms have been developed, facilitating cutting-edge research across many biochemical fields. However, despite considerable technological advancements, these systems remain limited in flexibility and chemical capability. Herein, we present a fully automated programmable platform that combines the efficiency of SPPS with the chemical flexibility of a Chemical Processing Unit (Chemputer). SPPS protocols, from resin swelling to peptide precipitation, are captured and automated using the Chemical Description Language (χDL), affording peptide sequences in high purity (>79%) and on a multi-milligram scale. Owing to the modularity of the platform, valuable transformations are integrated into the workflow, including ring-closing metathesis, copper-catalyzed azide-alkyne cycloaddition, and native chemical ligation. These tailored modifications are carried out in one, uninterrupted synthetic protocol, performing up to 1635-unit operations, executed over 85 h of activity, producing peptides such as GHRH(1-29), Semaglutide, and Capitellacin, finally unlocking bottlenecks in automated SPPS.
Authors
- Tristan J. Tyler (ORCID: https://orcid.org/0000-0003-3461-7968)
- Leroy Cronin (ORCID: https://orcid.org/0000-0001-8035-5757)
- Jacopo Zero (ORCID: https://orcid.org/0000-0002-6336-8414)
Institutions
- University of Glasgow (GB)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-08-08
- DOI
- https://doi.org/10.1038/s41467-025-62344-2
- Citations
- 6
- Primary Topic
- Chemical Synthesis and Analysis
- Type
- article
- Field-Weighted Citation Impact
- 4.84
Funders
- University of Glasgow
- National Institutes of Health
- Engineering and Physical Sciences Research Council