Evidence map›Paper›PMID 37258712›Full record

ArticleCommunications chemistry2023

Identification of photocrosslinking peptide ligands by mRNA display.

Yuteng Wu, M Teresa Bertran, Dhira Joshi, Sarah L Maslen, Catherine Hurd, Louise J Walport

Abstract read
In one paragraph

Article in Communications chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Covalent chemical probes.Communications chemistry · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Rapid capture of small peptide binders.Nature reviews. Chemistry · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Yuteng Wu *Protein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.ORCID http://orcid.org/0000-0002-8573-9626
M Teresa Bertran *Protein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.ORCID http://orcid.org/0000-0002-8336-0903
Dhira JoshiChemical Biology, The Francis Crick Institute, London, NW1 1AT, UK.
Sarah L MaslenProteomics, The Francis Crick Institute, London, NW1 1AT, UK.
Catherine HurdProtein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.ORCID http://orcid.org/0000-0001-6213-6809
Louise J WalportProtein-Protein Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK. l.walport@imperial.ac.uk.ORCID http://orcid.org/0000-0002-3795-8365

Funding

Wellcome Trust CC2030
6 · The paper itself

Abstract

Photoaffinity labelling is a promising method for studying protein-ligand interactions. However, obtaining a specific, efficient crosslinker can require significant optimisation. We report a modified mRNA display strategy, photocrosslinking-RaPID (XL-RaPID), and exploit its ability to accelerate the discovery of cyclic peptides that photocrosslink to a target of interest. As a proof of concept, we generated a benzophenone-containing library and applied XL-RaPID screening against a model target, the second bromodomain of BRD3. This crosslinking screening gave two optimal candidates that selectively labelled the target protein in cell lysate. Overall, this work introduces direct photocrosslinking screening as a versatile technique for identifying covalent peptide ligands from mRNA display libraries incorporating reactive warheads.

Identifiers

PMID37258712
PMCPMC10232439

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LicenceCC BY
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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.