Evidence map›Paper›PMID 40502689›Full record

ArticleiScience2025

Computational design of diverse nuclear factor erythroid 2 activators with cellular antioxidative activity.

Mingyue Yuwen, Xiaoning Gao, Junli Ba, Jiayang Wu, Jun Kang, Sheng Ye, Cheng Zhu

Abstract read
In one paragraph

Article in iScience, 2025. 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.

Mingyue YuwenState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Xiaoning GaoState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Junli BaState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Jiayang WuState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Jun KangState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Sheng YeState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Cheng ZhuState Key Laboratory of Synthetic Biology, Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress disrupts signaling pathways contributing to chronic diseases, while the KEAP1-NRF2 pathway is central to cellular antioxidant defenses. Current synthetic antioxidants struggle to activate this pathway efficiently or selectively. In this study, we employed deep learning algorithms to design miniproteins capable of activating NRF2. Five designed binders potently interfered with the KEAP1-NRF2 complex, exhibiting affinities ranging from 4.4 nM to 53.3 nM toward KEAP1. Two of these binders, designed through the motif scaffolding method, activated NRF2 in eukaryotic cells increasing antioxidant gene expression 3.8-fold and boosting cell survival across oxidative stress levels. Our approach illustrates the potential of integrated deep learning models to develop stable miniproteins that exhibit a variety of structural frameworks and thermodynamic characteristics. These designs hold promise for countering the cumulative effects of oxidative damage and for supporting the establishment of adaptive homeostasis within key antioxidative systems.

Indexed as

Biomolecular engineeringMolecular interactionProtein structure aspects

Identifiers

PMID40502689
PMCPMC12158508

What OpenQuestion holds

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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.