Evidence map›Paper›PMID 40014761›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025

Optimal Stapling of a Helical Peptide-Foldamer Hybrid Using a C-Terminal 4-Mercaptoproline Enhances Protein Surface Recognition and Cellular Activity.

Maxime Neuville, Mathieu Bourgeais, Jérémie Buratto, Claire Saragaglia, Bo Li, Isabel Galeano-Otero, Laura Mauran, Laetitia Varajao, Sébastien R Goudreau, Brice Kauffmann and 4 more

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. A General Synthesis Approach to Double-Guanidinium Stapled Peptides and Foldamers.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  3. Article
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

14 authors.

Maxime NeuvilleUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.
Mathieu BourgeaisUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0002-6347-2190
Jérémie BurattoUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.
Claire SaragagliaUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0002-9686-8992
Bo LiUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0003-4615-6898
Isabel Galeano-OteroUniv. Bordeaux, INSERM, BRIC, U 1312, F-33000, Bordeaux, France.ORCID https://orcid.org/0000-0003-3219-4201
Laura MauranUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0001-8278-618X
Laetitia VarajaoUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.
Sébastien R GoudreauIMMUPHARMA BIOTECH SAS, 15 rue de Bruxelles, 75009, Paris, France.ORCID https://orcid.org/0000-0002-2803-876X
Brice KauffmannUniv. Bordeaux, CNRS, INSERM, IECB, UAR3033, US001, F-33600, Pessac, France.ORCID https://orcid.org/0000-0002-2932-3255
Emmanuelle ThinonUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0001-9248-5655
Morgane PascoUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0002-1556-2802
Abdel-Majid KhatibUniv. Bordeaux, INSERM, BRIC, U 1312, F-33000, Bordeaux, France.ORCID https://orcid.org/0000-0001-6957-0384
Gilles GuichardUniv. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, IECB, 2 rue Robert Escarpit, F-33600, Pessac, France.ORCID https://orcid.org/0000-0002-2584-7502

Funding

Agence Nationale de la Recherche ANR-15-CE07-0010Agence Nationale de la Recherche ANR-20-CE18-0038Association Nationale de la Recherche et de la TechnologieConseil Régional Aquitaine 2017-1R10115
6 · The paper itself

Abstract

Structural analysis of a co-crystal of a helically-folded peptide-foldamer hybrid in complex with hDM2 E3 ubiquitin ligase, revealed a unique orientation for the C-terminal proline with the pyrrolidine ring pointing backwards in the sequence, and suggested new opportunities for macrocyclization. In particular, we found that the C-terminal prolyl residue could be replaced by its (2S,4S)-4-mercaptoprolyl analogue for optimal bisthioether crosslinking with a cysteine residue installed at position 4 in the sequence. The resulting i,i+7 stapled peptide-foldamer is a high-affinity binder to hDM2, is cell permeable and restores the p53 signalling pathway in p53wt cancer cells. The co-crystal structure of hDM2 and the stapled peptide-foldamer hybrid was determined at 1.84 Å, fully validating the original design and further highlighting the potential of cis-4-mercaptoproline in the context of peptide and foldamer stapling.

Indexed as

PeptidesProlineProto-Oncogene Proteins c-mdm2Crystallography, X-RayHumansModels, MolecularTumor Suppressor Protein p53MDM2 protein, humanPeptidesProlineProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53FoldamersHelical structuresMacrocyclesPeptidomimeticsProtein-protein interactions

Identifiers

PMID40014761
PMCPMC11962346

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.