Synthesis of multi-module low density lipoprotein receptor class A domains with acid labile cyanopyridiniumylides (CyPY) as aspartic acid masking groups. Issue 4 (1st February 2023)

• Record Type: Journal Article
• Authors: Neumann, Kevin; Vujinovic, Alex; Kamara, Saidu; Zwicky, André; Baldauf, Simon; Bode, Jeffrey W.
• Is Part Of: RSC chemical biology. Volume 4:Issue 4(2023)
• Page Start: 292
• Page End: 299
• Publication Date: 2023-02-01
• Subjects: 572
• DOI: 10.1039/d2cb00234e
• Languages: English
• ISSNs: 2633-0679

Abstract

Abstract : Single and multi-module low density lipoprotein receptor class A domains (LA modules) were synthesized with new acid labile cyanopyridiniumylides (CyPY) as aspartic acid monomers, which do not form aspartimides during solid phase peptide synthesis. Abstract : Low-density lipoprotein receptor class A domains (LA modules) are common ligand-binding domains of transmembrane receptors of approximately 40 amino acids that are involved in several cellular processes including endocytosis of extracellular targets. Due to their wide-ranging function and distribution among different transmembrane receptors, LA modules are of high interest for therapeutic applications. However, the efficient chemical synthesis of LA modules and derivatives is hindered by complications, many arising from the high abundance of aspartic acid and consequent aspartimide formation. Here, we report a robust, efficient and general applicable chemical synthesis route for accessing such LA modules, demonstrated by the synthesis and folding of the LA3 and LA4 modules of the low-density lipoprotein receptor, as well as a heterodimeric LA3–LA4 constructed by chemical ligation. The synthesis of the aspartic acid-rich LA domain peptides is made possible by the use of cyanopyridiniumylides (CyPY) – reported here for the first time – as a masking group for carboxylic acids. We show that cyanopyridiniumylide masked aspartic acid monomers are readily available building blocks for solid phase peptide synthesis and successfully suppress aspartimide formation. Unlike previously reported ylide-based carboxylic acid protecting groups, CyPY protected aspartic acids are converted to the free carboxylic acid by acidic hydrolysis and are compatible with all common residues and protecting groups. The chemical synthesis of Cys- and Asp-rich LA modules enables new access to a class of difficult to provide, but promising protein domains.