Evidence map›Paper›PMID 41255251›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Amino Acid Directed Helical Assemblies of Natural Berberine for Chirality-Dependent Photodynamic Antibacterial Therapy.

Haoqiang Zhao, Jingyi Jiao, Zhixia Wang, Chengyu Shi, Xinran Huang, Yixuan Lin, Haolin Yang, Haimin Lei, Guanghui Ouyang, Minghua Liu

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

10 authors.

Haoqiang ZhaoSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Jingyi JiaoSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Zhixia WangSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Chengyu ShiSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Xinran HuangSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Yixuan LinSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Haolin YangSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Haimin LeiSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, 102488, China.
Guanghui OuyangBeijing National Laboratory of Molecular Sciences and CAS Key Laboratory of Colloid Interface and Thermodynamics, Institute of Chemistry Chinese Academy of Sciences, ZhongGuanCun North First Street 2, Beijing, 100190, China.
Minghua LiuBeijing National Laboratory of Molecular Sciences and CAS Key Laboratory of Colloid Interface and Thermodynamics, Institute of Chemistry Chinese Academy of Sciences, ZhongGuanCun North First Street 2, Beijing, 100190, China.ORCID https://orcid.org/0000-0002-6603-1251

Funding

Beijing Nova Program 20230484423National Natural Science Foundation of China 22322207National Natural Science Foundation of China 52321006National Natural Science Foundation of China 82304704
6 · The paper itself

Abstract

While the biological effects of chiral pharmaceuticals at molecular level have been extensively studied, research remains limited on how chiral materials derived from natural herbal components exert biomedical effects at higher hierarchical levels. Herein, it is reported that helical nanostructures co-assembled from a traditional Chinese medicine-derived berberine (BBR) and an amino acid derivative (Fmoc-Y) exhibit supramolecular-chirality-dependent photodynamic antibacterial activity. The inherent molecular chirality of the Fmoc-Y component directs the organization of achiral BBR into chiral nanofibers. The experimental results reveal that supramolecular chirality governs nanofiber adsorption on bacterial surfaces and subsequent membrane penetration. Compared with left-handed nanofibers, the chirality-matched right-handed ones enable more efficient intracellular delivery of BBR and reactive oxygen species (ROS) generation, leading to superior bacterial inhibition. This work highlights, for the first time, the unique role of supramolecular chirality in biomedicine applications based on natural herbal components, demonstrating how supramolecular chiral engineering synergizes with natural pharmacophores to develop high-efficiency antimicrobial systems and advanced theranostic platforms.

Indexed as

Amino AcidsAnti-Bacterial AgentsBerberinePhotochemotherapyHumansReactive Oxygen SpeciesStereoisomerismAmino AcidsAnti-Bacterial AgentsBerberineReactive Oxygen Speciesantibacterial activityberberinenanostructuresself‐assemblysupramolecular chirality

Identifiers

PMID41255251
PMCPMC12806354

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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.