Evidence map›Paper›PMID 41164298›Full record

ArticleChemical science2025

Aggregation of DNA oligomers with a neutral polymer facilitates DNA solubilization in organic solvents for DNA-encoded chemistry.

Johannes Bingold, Erik Mafenbayer, Wibke Langenkamp, Lisa Liang, Chun Zhang, Malte Mildner, Julia Isabel Bahner, Mohamed Akmal Marzouk, Bettina Böttcher, Ann-Christin Pöppler and 2 more

Abstract read
In one paragraph

Article in Chemical science, 2025. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

12 authors.

Johannes BingoldInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany andreas.brunschweiger@uni-wuerzburg.de.
Erik MafenbayerInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany andreas.brunschweiger@uni-wuerzburg.de.
Wibke LangenkampDepartment of Chemistry and Chemical Biology, Polymer Hybrid Systems, TU Dortmund University Otto-Hahn Straße 6 44227 Dortmund Germany.ORCID https://orcid.org/0009-0004-2807-2644
Lisa LiangInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany andreas.brunschweiger@uni-wuerzburg.de.
Chun ZhangInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany andreas.brunschweiger@uni-wuerzburg.de.
Malte MildnerInstitute of Organic Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany.ORCID https://orcid.org/0009-0006-0425-3656
Julia Isabel BahnerRudolf-Virchow-Center, Julius-Maximilians-Universität Würzburg Josef-Schneider-Straße 2 97080 Würzburg Germany.
Mohamed Akmal MarzoukInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany andreas.brunschweiger@uni-wuerzburg.de.
Bettina BöttcherRudolf-Virchow-Center, Julius-Maximilians-Universität Würzburg Josef-Schneider-Straße 2 97080 Würzburg Germany.ORCID https://orcid.org/0000-0002-7962-4849
Ann-Christin PöpplerInstitute of Organic Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany.ORCID https://orcid.org/0000-0002-0624-1708
Ralf WeberskirchDepartment of Chemistry and Chemical Biology, Polymer Hybrid Systems, TU Dortmund University Otto-Hahn Straße 6 44227 Dortmund Germany.ORCID https://orcid.org/0000-0002-8885-0530
Andreas BrunschweigerInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany andreas.brunschweiger@uni-wuerzburg.de.ORCID https://orcid.org/0000-0002-4401-1495

Funding

Wellcome Trust
6 · The paper itself

Abstract

Chemical diversification of DNA-conjugated substrates is key in DNA-encoded library (DEL) synthesis and other nucleic acid-based technologies. One major challenge to the translation of synthesis methods to DNA-tagged substrates is the lack of solubility of the highly charged DNA oligomer in most organic solvents. A neutral acrylate block copolymer, devoid of any canonical nucleic acid-binding structure, tightly interacted with DNA oligonucleotides in their ammonium form, and solubilized them in nonpolar solvents such as dichloromethane, chloroform and toluene. The ternary DNA-copolymer-ammonium salt interactions led to the formation of aggregates in organic solvents whose size correlated with DNA oligomer length. This method for DNA solubilization was successfully applied to diversify DNA-tagged starting materials by three isocyanide multicomponent reactions (IMCR) with broad scope and excellent yields. The copolymer does not require tailored DNA conjugates and solubilized DNA oligomers of up to 80 nucleotides length. It will likely broaden the toolbox of DEL-compatible synthesis methods well beyond IMCR chemistry and it has application potential in other nucleic acid-based technologies that require a broadened solvent scope for nucleic acid conjugate synthesis.

Identifiers

PMID41164298
PMCPMC12560349

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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.