Library‐on‐Library Intercellular Labeling for Selection of Biotin Ligase and Acceptor Peptides

Library-on-library (LOL) selection screens combinatorial libraries to generate new protein pairs. Previously, LOL selection has only been applied to stable protein-protein interactions. To extend LOL to transient enzyme-substrate pairs, a generalizable sequential LOL trans- and cis-labeling platform is developed, and a proof-of-concept selection is performed on Escherichia coli biotin ligase (BirA) and its acceptor peptide (AP). Using yeast surface display, AP mutant libraries are selected against BirA mutant libraries to identify AP variants trans-biotinylated by BirA mutants. Matched BirA mutants are subsequently enriched via the SpyTag-SpyCatcher-mediated cis-labeling platform. This represents the first demonstration of enzyme-peptide substrate LOL selection and offers a versatile framework for engineering new enzyme-peptide substrate pairs with varied activities.

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Publication Details

Journal
ChemBioChem
Published
2026-01-01
DOI
https://doi.org/10.1002/cbic.202500804
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
0.00

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article

Library‐on‐Library Intercellular Labeling for Selection of Biotin Ligase and Acceptor Peptides

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article

Library‐on‐Library Intercellular Labeling for Selection of Biotin Ligase and Acceptor Peptides

Benya Lakkanasirorat, Rawiporn Amornloetwattana, Chayasith Uttamapinant, Wenjing Wang, Pansa Leejareon, Phatipon Kongkamnead
article en

Abstract

Library-on-library (LOL) selection screens combinatorial libraries to generate new protein pairs. Previously, LOL selection has only been applied to stable protein-protein interactions. To extend LOL to transient enzyme-substrate pairs, a generalizable sequential LOL trans- and cis-labeling platform is developed, and a proof-of-concept selection is performed on Escherichia coli biotin ligase (BirA) and its acceptor peptide (AP). Using yeast surface display, AP mutant libraries are selected against BirA mutant libraries to identify AP variants trans-biotinylated by BirA mutants. Matched BirA mutants are subsequently enriched via the SpyTag-SpyCatcher-mediated cis-labeling platform. This represents the first demonstration of enzyme-peptide substrate LOL selection and offers a versatile framework for engineering new enzyme-peptide substrate pairs with varied activities.

ChemBioChemVol. 27(1)
Washtenaw Community College (US), University of Michigan (US), Vidyasirimedhi Institute of Science and Technology (TH)
Vidyasirimedhi Institute of Science and Technology
Openalex Percentile: Top 92%
Biochemical and Structural Characterization
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