A Versatile “Synthesis Tag” (SynTag) for the Chemical Synthesis of Aggregating Peptides and Proteins

Solid-phase peptide synthesis (SPPS) and native chemical ligation (NCL) are powerful methods for obtaining peptides and proteins that are otherwise inaccessible. Nonetheless, numerous sequences are difficult to prepare via SPPS, and cleaved peptides often have low aqueous solubility. To address these challenges, we developed a "Synthesis Tag" consisting of six arginines connected to the target sequence via a cleavable MeDbz linker. "SynTag" effectively improves batch- and flow-SPPS of "difficult sequences", enhances the solubility of the cleaved peptides, and provides direct access to native sequences by hydrolysis, or peptide thioesters for NCL. We demonstrate its utility in the first chemical synthesis of the MYC transactivation domain with a single NCL. We envisage SynTag to become a broadly applicable tool that enables the synthesis and study of previously unattainable peptides and proteins.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-12-06
DOI
https://doi.org/10.1021/jacs.4c14247
Citations
22
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
5.14

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article

A Versatile “Synthesis Tag” (SynTag) for the Chemical Synthesis of Aggregating Peptides and Proteins

Elyse T. Williams, Robin Lescure, Nina Hartrampf, Adhvitha Premanand et al.
22 citations
Journal of the American Chemical Society
Chemical Synthesis and Analysis
5.14
article

A Versatile “Synthesis Tag” (SynTag) for the Chemical Synthesis of Aggregating Peptides and Proteins

Elyse T. Williams, Robin Lescure, Nina Hartrampf, Adhvitha Premanand, Aliénor Jeandin, H Burgisser, Songlin Wang
article en
22 citations

Abstract

Solid-phase peptide synthesis (SPPS) and native chemical ligation (NCL) are powerful methods for obtaining peptides and proteins that are otherwise inaccessible. Nonetheless, numerous sequences are difficult to prepare via SPPS, and cleaved peptides often have low aqueous solubility. To address these challenges, we developed a "Synthesis Tag" consisting of six arginines connected to the target sequence via a cleavable MeDbz linker. "SynTag" effectively improves batch- and flow-SPPS of "difficult sequences", enhances the solubility of the cleaved peptides, and provides direct access to native sequences by hydrolysis, or peptide thioesters for NCL. We demonstrate its utility in the first chemical synthesis of the MYC transactivation domain with a single NCL. We envisage SynTag to become a broadly applicable tool that enables the synthesis and study of previously unattainable peptides and proteins.

Journal of the American Chemical SocietyVol. 146(50)
University of Wisconsin–Madison (US), University of Zurich (CH)
National Science Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Ministerio de Ciencia e Innovación, Universität Zürich
Zero hunger
Openalex Percentile: Top 4%
Chemical Synthesis and Analysis
5.14
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