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.

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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

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article

Universal peptide synthesis via solid-phase methods fused with chemputation

Tristan J. Tyler, Leroy Cronin, Jacopo Zero
6 citations
Nature Communications
Chemical Synthesis and Analysis
4.84
article

Universal peptide synthesis via solid-phase methods fused with chemputation

Tristan J. Tyler, Leroy Cronin, Jacopo Zero
article en
6 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
University of Glasgow (GB)
University of Glasgow, National Institutes of Health, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 5%
Chemical Synthesis and Analysis
4.84
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