Evidence map›Paper›PMID 41873756›Full record

ArticleNucleic acids research2026

Deep learning-guided dual-fitness evolution of T7 RNA polymerase for enhanced stability and activity.

Fan Jiang, Liqi Kang, Mingchen Li, Bozitao Zhong, Xiaoxia Chen, Banghao Wu, Mengrong Li, Yuanxi Yu, Liang Hong

Abstract read
In one paragraph

Article in Nucleic acids research, 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
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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

9 authors.

Fan JiangInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.ORCID 0000-0002-9727-853X
Liqi KangInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.
Mingchen LiInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.
Bozitao ZhongZhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 201203, China.
Xiaoxia ChenInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.
Banghao WuZhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 201203, China.
Mengrong LiInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.
Yuanxi YuInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.
Liang HongInstitute of Natural Sciences & School of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China.

Funding

Computational Biology Key Program of Shanghai Science and Technology Commission 23JS1400600National Key Research and Development Program of China 2024YFA0917603Science and Technology Innovation Key R&D Program of Chongqing CSTB2022TIAD-STX0017Science and Technology Innovation Key R&D Program of Chongqing CSTB2024TIAD-STX0032Shanghai Artificial Intelligence LaboratoryShanghai Jiao Tong University Scientific and Technological Innovation Funds 21X010200843Shanghai Municipal Commission of Economy and Informatization 2025-GZL-RGZN-BTBX-02009Shanghai Municipal Science and Technology Major ProjectStudent Innovation Center at Shanghai Jiao Tong University
6 · The paper itself

Abstract

In protein engineering, simultaneously improving multiple fitness attributes is a critical yet challenging goal, largely due to the vastness of sequence space, the multifaceted interplay among different traits, and the complexity of non-linear mutational effects (epistasis). To address this, we developed a data-driven evolutionary strategy that couples in silico deep learning with a wet-lab multi-objective selection workflow. By employing independent model fine-tuning for distinct traits, our approach facilitates navigating the fitness landscape to identify beneficial mutation combinations. We applied this strategy to T7 RNA polymerase (T7 RNAP), performing dual-fitness evolution to simultaneously enhance thermostability and activity at elevated temperatures. After five rounds of iterative evolution, we obtained T7 RNAP mutants exhibiting a melting temperature (Tm) increase of >10°C, a 60-fold enhancement in high-temperature activity, and a 70% reduction in by-product content. Validation in cell transfection demonstrated their potential for producing high-quality mRNA for industrial applications.

Indexed as

Deep LearningDirected Molecular EvolutionDNA-Directed RNA PolymerasesProtein EngineeringViral ProteinsBacteriophage T7Enzyme StabilityMutationbacteriophage T7 RNA polymeraseDNA-Directed RNA PolymerasesViral Proteins

Identifiers

PMID41873756
PMCPMC13010154

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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.