Evidence map›Paper›PMID 40663320›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2025

DNA-Encoded Peptide Library Synthesis and Applications, a Mini-Review.

Stefan M Matysiak, Klaus Hellmuth

Abstract readReview
PubMed Publisher
In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 2025. 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

2 authors.

Stefan M MatysiakLagoBiotech Consulting, Lindau, Berlin, Germany. s.matysiak@lagobiotech.com.
Klaus HellmuthLagoBiotech Consulting, Lindau, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA-encoded chemical libraries (DECLs) are an innovative technology that combines molecular biology and combinatorial chemistry to create and screen vast libraries of small molecules and peptides. DECLs, including DNA-encoded peptide libraries (DEPLs), leverage DNA as a molecular barcode, enabling the identification of binders through affinity selection and sequencing. Advanced techniques, such as DNA-encoded self-assembled chemical libraries (DESACLs), enhance library diversity by using DNA hybridization and self-assembly to produce dual pharmacophores, significantly advancing fragment-based drug discovery.The modular nature of DESACLs allows for dynamic assembly and combinatorial expansion, generating libraries with millions of combinations. This approach supports drug discovery by targeting complex biological interactions, such as protein-protein interfaces and provides a platform for molecular diagnostics.

Indexed as

DNAPeptide LibraryPeptidesCombinatorial Chemistry TechniquesDrug DiscoveryHumansNucleic Acid HybridizationSmall Molecule LibrariesDNAPeptide LibraryPeptidesSmall Molecule LibrariesCombinatorial chemistryCombinatorial hybridizationDNA-encoded chemical librariesDNA-encoded peptide librariesDNA-encoded self-assembled libraries

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.