Incorporation of Aliphatic Proline Residues into Recombinantly Produced Insulin

Stephanie L. Breunig, Janine C. Quijano, Cecile Donohue, Amy Henrickson, Borries Demeler, Hsun Teresa Ku, David A. Tirrell

Research output: Contribution to journalArticlepeer-review

Abstract

Analogs of proline can be used to expand the chemical space about the residue while maintaining its uniquely restricted conformational space. Here, we demonstrate the incorporation of 4R-methylproline, 4S-methylproline, and 4-methyleneproline into recombinant insulin expressed in Escherichia coli. These modified proline residues, introduced at position B28, change the biophysical properties of insulin: Incorporation of 4-methyleneproline at B28 accelerates fibril formation, while 4-methylation speeds dissociation from the pharmaceutically formulated hexamer. This work expands the scope of proline analogs amenable to incorporation into recombinant proteins and demonstrates how noncanonical amino acid mutagenesis can be used to engineer the therapeutically relevant properties of protein drugs.

Original languageEnglish
Pages (from-to)2574-2581
Number of pages8
JournalACS Chemical Biology
Volume18
Issue number12
DOIs
StatePublished - Dec 15 2023

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