Evidence map›Paper›PMID 41981101›Full record

ReviewExperimental & molecular medicine2026

Biomimetic peptide self-assembly: interfacing with biomacromolecules to regulate cellular signaling.

Dohyun Kim, Gaeun Park, Min-Seok Seu, Injun Hwang, Sanjay Kumar Perumandla, Jaemo Lee, Ja-Hyoung Ryu

Abstract readReview
In one paragraph

Review in Experimental & molecular medicine, 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

7 authors.

Dohyun Kim *Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Gaeun Park *Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Min-Seok Seu *Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Injun HwangDepartment of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Sanjay Kumar PerumandlaDepartment of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Jaemo LeeDepartment of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Ja-Hyoung RyuDepartment of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea. jhryu@unist.ac.kr.ORCID http://orcid.org/0000-0003-0252-0985

Funding

National Research Foundation of Korea (NRF) 2020M3A9D8038192National Research Foundation of Korea (NRF) RS-2023-00208386National Research Foundation of Korea (NRF) RS-2023-00281553
6 · The paper itself

Abstract

Supramolecular self-assembly represents a spontaneous and reversible process that bridges discrete molecular building blocks with nanoscale architecture through non-covalent interactions. By rationally tuning these interactions, diverse nanostructures can be precisely constructed, each exhibiting distinct physicochemical and functional properties. The dynamic and multivalent nature of supramolecular assemblies endows them with structural adaptability and cooperative binding, enabling responsiveness to environmental cues and amplification of weak molecular interactions. Nature provides abundant paradigms for such self-organization, in which organized supramolecular interfaces mediate complex biological functions. Inspired by these natural principles, artificial self-assembly systems have been engineered to emulate the hierarchical organization and functional adaptability of living systems. In this Review, we summarize recent advances in nature-inspired supramolecular assemblies, focusing on peptide-based systems that exploit the chemical diversity of amino acids to modulate biomacromolecular interactions and cellular signaling. Understanding these biomimetic design principles offers a foundation for developing next-generation functional materials that bridge molecular precision with biological functionality.

Indexed as

Biomimetic MaterialsBiomimeticsPeptidesSignal TransductionAnimalsHumansNanostructuresPeptides

Identifiers

PMID41981101
PMCPMC13144528

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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.