Evidence map›Paper›PMID 41767808›Full record

ArticleChemical science2026

One-pot multi-substrate screening of ligation reactions using PNA tags.

Aki Kohyama, Sofia Barluenga, Nicolas Winssinger

Abstract read
In one paragraph

Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Aki KohyamaDepartment of Organic Chemistry, Faculty of Sciences, University of Geneva Geneva 12004 Switzerland koyama.aki.6a@kyoto-u.ac.jp Nicolas.Winssinger@unige.ch.ORCID https://orcid.org/0000-0002-3884-858X
Sofia BarluengaDepartment of Organic Chemistry, Faculty of Sciences, University of Geneva Geneva 12004 Switzerland koyama.aki.6a@kyoto-u.ac.jp Nicolas.Winssinger@unige.ch.ORCID https://orcid.org/0000-0003-3830-1178
Nicolas WinssingerDepartment of Organic Chemistry, Faculty of Sciences, University of Geneva Geneva 12004 Switzerland koyama.aki.6a@kyoto-u.ac.jp Nicolas.Winssinger@unige.ch.ORCID https://orcid.org/0000-0003-1636-7766

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemical ligation is an essential tool for constructing complex biomolecular architectures. To accelerate reaction discovery, a one-pot multi-substrate screening (OPMSS) platform was developed, combining peptide nucleic acid (PNA) tagging with direct MALDI analysis. This approach enables the simultaneous evaluation of multiple substrate pairs in a single pot without the need for chromatographic separation. Short PNA tags promote a uniform combinatorial pairing of substrates while the neutral polyamide backbone facilitates MALDI analysis to allow direct readout of ligated products as predominantly singly charged ions. Using this system, we readily detected established ligations, including Huisgen cycloaddition and amide bond formation, validating the platform in pilot screens pairing 8 × 8 substrates (64 possible combinations). Applying the method to discovery-mode screening of 13 × 11 substrates under visible-light photocatalytic conditions identified a previously unexplored ligation between alkyl azides and alkenes, consistent with pathways involving aminyl radicals or aminium radical cations. This work demonstrates the potential of OPMSS with PNA tagging as a practical and discovery-oriented approach for identifying new ligation reactions directly from complex mixtures.

Identifiers

PMID41767808
PMCPMC12937129

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.