Primer Extension-MediatedAptamer-Gated DNA-EncodedLibrary Screening for Physiologically Relevant Ligand Discovery

DNA-encoded library (DEL) technologies have revolutionized drug discovery, yet their reliance on purified targets often yields ligands with a poor physiological relevance. Here, we introduce Primer Extension-Mediated Aptamer-Gated DEL Screening (PEMAG-DEL), a transformative platform that integrates aptamer-guided target localization, enzymatic fidelity filtering, and combinatorial chemistry to enable ligand discovery in native-like environments. We selected carbonic anhydrase II (CA II) as a model target and designed a 125-member DEL library composed of peptide–sulfonamide conjugates to perform screening and selection using the PEMAG-DEL platform. As a result, we identified a high-affinity ligand, Sulfo–His–His–Ala, which exhibited a 16.3-fold improvement in binding affinity (IC<sub>50</sub> = 0.84 μM) compared to the parent compound, 4-sulfobenzoic acid. PEMAG-DEL screening in HeLa cell lysates demonstrated robust resistance to nonspecific interference from membrane proteins and aggregates. These findings confirm that PEMAG-DEL enables precise selection of biologically relevant ligands even in complex, native-like environments.

Publication Details

Journal
Figshare
Published
2025-07-23
DOI
https://doi.org/10.1021/acs.jmedchem.5c01151.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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Primer Extension-MediatedAptamer-Gated DNA-EncodedLibrary Screening for Physiologically Relevant Ligand Discovery

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Mycorrhizal Fungi and Plant Interactions
article

Primer Extension-MediatedAptamer-Gated DNA-EncodedLibrary Screening for Physiologically Relevant Ligand Discovery

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Abstract

DNA-encoded library (DEL) technologies have revolutionized drug discovery, yet their reliance on purified targets often yields ligands with a poor physiological relevance. Here, we introduce Primer Extension-Mediated Aptamer-Gated DEL Screening (PEMAG-DEL), a transformative platform that integrates aptamer-guided target localization, enzymatic fidelity filtering, and combinatorial chemistry to enable ligand discovery in native-like environments. We selected carbonic anhydrase II (CA II) as a model target and designed a 125-member DEL library composed of peptide–sulfonamide conjugates to perform screening and selection using the PEMAG-DEL platform. As a result, we identified a high-affinity ligand, Sulfo–His–His–Ala, which exhibited a 16.3-fold improvement in binding affinity (IC<sub>50</sub> = 0.84 μM) compared to the parent compound, 4-sulfobenzoic acid. PEMAG-DEL screening in HeLa cell lysates demonstrated robust resistance to nonspecific interference from membrane proteins and aggregates. These findings confirm that PEMAG-DEL enables precise selection of biologically relevant ligands even in complex, native-like environments.

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Mycorrhizal Fungi and Plant Interactions
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Primer Extension-MediatedAptamer-Gated DNA-EncodedLibrary Screening for Physiologically Relevant Ligand Discovery · Figshare (2025) | TGRS Research Map | TGRS