Evidence map›Paper›PMID 41934180›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026

Click Capture SELEX for the Identification of Click-Modified Aptamers Targeting Small Molecules in Solution.

Philipp Menke, Carmelo Di Primo, Felix Bernhardt, Alea Schröder, Christian Renzl, Günter Mayer

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

6 authors.

Philipp MenkeLife and Medical Science Institute (LIMES), University of Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0003-3134-7931
Carmelo Di PrimoCNRS, INSERM, ARNA, UMR 5320, U1212, European Institute of Chemistry and Biology, University of Bordeaux, Pessac, France.
Felix BernhardtLife and Medical Science Institute (LIMES), University of Bonn, Bonn, Germany.
Alea SchröderLife and Medical Science Institute (LIMES), University of Bonn, Bonn, Germany.
Christian RenzlLife and Medical Science Institute (LIMES), University of Bonn, Bonn, Germany.
Günter MayerLife and Medical Science Institute (LIMES), University of Bonn, Bonn, Germany.

Funding

European Innovation Council 101099652
6 · The paper itself

Abstract

Capture SELEX is an in vitro selection method used to identify aptamers that bind small molecules in solution. The interaction of aptamers with their targets is primarily determined by supramolecular interactions, which are constrained by the chemical diversity of the canonical nucleobases. To overcome this limitation, the interaction properties of nucleic acid libraries can be expanded using nucleobase modifications. We developed click capture SELEX for the purpose of enriching chemically modified aptamers, also referred to as clickmers, which bind to small molecules. In this study, an indole-modified DNA library was utilized to identify clickmers that bind specifically to kanamycin A. The click capture SELEX approach was employed to identify clickmers that bind small molecules in solution, thereby overcoming common limitations associated with using immobilized small target molecules in SELEX. The method described herein is generally adaptable to various small molecules.

Indexed as

Aptamers, NucleotideKanamycinSELEX Aptamer TechniqueSmall Molecule LibrariesClick ChemistryGene LibraryIndolesSolutionsAptamers, NucleotideIndolesKanamycinSmall Molecule LibrariesSolutionsaptamerCuAACmethod developmentnucleobase modificationsSELEX

Identifiers

PMID41934180
PMCPMC13282910

What OpenQuestion holds

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Registered trials

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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.