Evidence map›Paper›PMID 42434462›Full record

ArticleACS materials Au2026

Synergistic Multicomponent Nucleopeptide-Based Hydrogels: Harnessing DNA-Base Pairing and Electrostatic Complementarities.

Tristan Giraud, Marine Koch, Paul Hoschtettler, Guillaume Pickaert, Marie-Christine Averlant-Petit, Loïc Stefan

Abstract read
In one paragraph

Article in ACS materials Au, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Rheological Modeling to Assess the Gelation Kinetics of Mono- and Multicomponent Supramolecular Hydrogels.Chemphyschem : a European journal of chemical physics and physical chemistry · 2026
    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

6 authors.

Tristan GiraudUniversité de Lorraine, CNRS, LCPM, F-54000 Nancy, France.
Marine KochUniversité de Lorraine, CNRS, LCPM, F-54000 Nancy, France.
Paul HoschtettlerUniversité de Lorraine, CNRS, LCPM, F-54000 Nancy, France.ORCID https://orcid.org/0000-0001-9473-9129
Guillaume PickaertUniversité de Lorraine, CNRS, LCPM, F-54000 Nancy, France.
Marie-Christine Averlant-PetitUniversité de Lorraine, CNRS, LCPM, F-54000 Nancy, France.
Loïc StefanUniversité de Lorraine, CNRS, LCPM, F-54000 Nancy, France.ORCID https://orcid.org/0000-0001-8517-5982

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydrogels are everyday materials characterized by their remarkable properties, of bridging the gap between liquid and solid states. While most hydrogels are traditionally formed from polymers, biomolecules can also undergo gelation, as seen with proteins (e.g., collagen), enabling numerous applications. Peptide-based low-molecular-weight hydrogels (LMWHs), composed of amino acids, have emerged as innovative materials with a broad range of biomedical and biotechnological applications, gaining commercial interest in the 2010s. However, natural peptides composed solely of proteinogenic amino acids present several drawbacks, requiring structural or chemical modifications to enhance their performance. Additionally, multicomponent approaches, which involve combining multiple compounds to form hydrogels, have recently gained prominence as a promising strategy for developing more versatile and efficient systems. In this context, we explore emerging hybrid molecules, i.e., peptides functionalized with DNA bases (i.e., adenine, thymine, guanine, and cytosine), known as nucleopeptides. These compounds have shown encouraging results, yet much remains to be explored to unlock their full potential. In this study, we present a novel series of six (nucleo)-peptides derived from two distinct peptide sequences, Phe-Glu-Phe-Glu and Phe-Lys-Phe-Lys, negatively and positively charged at physiological pH, respectively, making them complementary in terms of electrostatic interactions. These peptides are functionalized with one of the four DNA nucleobases, introduced via a peptide nucleic acid (PNA) moiety. Thus, through a comprehensive multiscale systematic study, we report herein on the impact of charge complementarity and/or nucleobase-pair complementarity on the mechanical and physicochemical properties of the resulting multicomponent hydrogels (including gelation time, sol-gel transition temperature, stiffness, resistance to external stress, fibrillar network morphology, etc.). Then, the results highlight the undeniable potential of this approach, demonstrating that careful selection of components allows the fine-tuning of hydrogel properties. Interestingly, our findings reveal unexpected behaviors, underscoring the complexity of these bioinspired hybrid multicomponent systems while reinforcing their potential for the development of high-performance and innovative supramolecular hydrogels.

Indexed as

DNA nucleobasemulticomponent hydrogelsmultiscale analysisnucleopeptiderheologysupramolecular hydrogelssynergistic supramolecular assembly

Identifiers

PMID42434462
PMCPMC13352277

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.