Evidence map›Paper›PMID 42458029›Full record

ReviewNature reviews. Chemistry2026

Bridging stimulus-responsive and dissipative peptide assemblies to build complex interactive biomaterials.

Maximilian Schuler, Ayan Chatterjee, David Y W Ng, Tanja Weil

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Chemistry, 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

4 authors.

Maximilian SchulerMax Planck Institute for Polymer Research, Mainz, Germany.
Ayan ChatterjeeMax Planck Institute for Polymer Research, Mainz, Germany.
David Y W NgMax Planck Institute for Polymer Research, Mainz, Germany. david.ng@mpip-mainz.mpg.de.ORCID 0000-0002-0302-0678
Tanja WeilMax Planck Institute for Polymer Research, Mainz, Germany. weil@mpip-mainz.mpg.de.ORCID 0000-0002-5906-7205

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Self-assembling peptides are versatile building blocks for biomaterials owing to their programmable sequences and ability to form complex supramolecular architectures. Designing systems that operate dynamically at the biological interface is particularly compelling, as living systems rely on both stimulus responsiveness and continuous energy dissipation to regulate structure and function. However, most synthetic peptide assemblies remain confined to near-equilibrium behaviour, whereas chemically fuelled dissipative systems often lack compatibility with biological environments. In this Review, we discuss recent advances in stimulus-responsive and dissipative peptide assemblies, highlighting their distinct design principles and functional capabilities. We compare sequence-encoded and trigger-based strategies with chemically fuelled reaction networks that enable transient assembly. Finally, we outline emerging strategies to bridge these approaches, including improving bioorthogonality, tuning concentration regimes, and integrating cellular processes. Together, these concepts provide a framework for developing interactive peptide biomaterials with life-like functions.

Indexed as

Biocompatible MaterialsPeptidesAnimalsHumansBiocompatible MaterialsPeptides

Identifiers

PMID42458029

What OpenQuestion 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 OpenQuestion graph.