A designer enzyme for hydrazone and oxime formation featuring an unnatural catalytic aniline residue

Ivana Drienovská, Clemens Mayer, Christopher Dulson, Gerard Roelfes*

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Creating designer enzymes with the ability to catalyse abiological transformations is a formidable challenge. Efforts toward this goal typically consider only canonical amino acids in the initial design process. However, incorporating unnatural amino acids that feature uniquely reactive side chains could significantly expand the catalytic repertoire of designer enzymes. To explore the potential of such artificial building blocks for enzyme design, here we selected p-aminophenylalanine as a potentially novel catalytic residue. We demonstrate that the catalytic activity of the aniline side chain for hydrazone and oxime formation reactions is increased by embedding p-aminophenylalanine into the hydrophobic pore of the multidrug transcriptional regulator from Lactococcus lactis. Both the recruitment of reactants by the promiscuous binding pocket and a judiciously placed aniline that functions as a catalytic residue contribute to the success of the identified artificial enzyme. We anticipate that our design strategy will prove rewarding to significantly expand the catalytic repertoire of designer enzymes in the future.

Original languageEnglish
Pages (from-to)946-952
Number of pages7
JournalNature Chemistry
Volume10
Issue number9
DOIs
Publication statusPublished - 1 Sept 2018
Externally publishedYes

Funding

This project was supported by the European Research Council (ERC starting grant no. 280010) and the Netherlands Organisation for Scientific Research (NWO) (Vici grant 724.013.003, and Veni grant 722.017.007). G.R. acknowledges support from the Ministry of Education Culture and Science (Gravitation programme no. 024.001.035). C.M. acknowledges a Marie Skłodowska Curie Individual Fellowship (project no. 751509). The authors thank A. Borg for preparing the plasmid harbouring the bcPadR1 gene and M. de Vries for performing trypsin digestion and LC–MS/MS analyses.

FundersFunder number
Ministry of Education Culture and Science024.001.035
Horizon 2020 Framework Programme751509
European Research Council280010
Nederlandse Organisatie voor Wetenschappelijk Onderzoek724.013.003, 722.017.007

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