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

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

PMC · DOI: 10.1093/nar/gkag259 · 2026-03-24

## TL;DR

This paper introduces a deep learning-guided method to evolve T7 RNA polymerase for better stability and activity at high temperatures.

## Contribution

A novel data-driven evolutionary strategy combining deep learning and multi-objective wet-lab selection for dual-fitness protein engineering.

## Key findings

- T7 RNAP mutants showed a melting temperature increase of over 10°C.
- High-temperature activity improved 60-fold with a 70% reduction in by-products.
- Mutants validated for high-quality mRNA production in cell transfection.

## 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.

Graphical Abstract

## Full-text entities

- **Genes:** CAP1 (cyclase associated actin cytoskeleton regulatory protein 1) [NCBI Gene 10487] {aka CAP, CAP1-PEN}, NUSAP1 (nucleolar and spindle associated protein 1) [NCBI Gene 51203] {aka ANKT, BM037, LNP, NUSAP, PRO0310p1, Q0310}
- **Chemicals:** M1 (MESH:C400939), ethanol (MESH:D000431), Triton X-100 (MESH:D017830), imidazole (MESH:C029899), 1,2-distearoyl-sn-glycero-3-phosphocholine (MESH:C010942), cholesterol (MESH:D002784), SM102 (MESH:C000712867), DMEM (-), 3,5-difluoro-4-hydroxybenzylidene imidazolinone (MESH:C560120), streptomycin (MESH:D013307), hydrogen (MESH:D006859), spermidine (MESH:D013095), Lipids (MESH:D008055), HEPES (MESH:D006531), EDTA (MESH:D004492), glycerol (MESH:D005990), ampicillin (MESH:D000667), MgCl2 (MESH:D015636), penicillin (MESH:D010406), DMG-PEG-2000 (MESH:C000626005), FAM (MESH:C031179), acetate (MESH:D000085), nucleotide (MESH:D009711), 3,3',5,5'-tetramethylbenzidine (MESH:C021758), NaCl (MESH:D012965), water (MESH:D014867), DTT (MESH:D004229), glycine (MESH:D005998), CO2 (MESH:D002245), kanamycin (MESH:D007612)
- **Mutations:** M306K, W797L, K642G, Y846R, A468F, A881F, S430P, S633P, P780K, V567P, P865L, Q269M, Q786L, A703T, C510E, H799G, S397W, R792M, L665D, C515P, W422F, N601E, M696A, P476E, E830G, P742G, N529V, T375K, M369T, A124N, S606V, G618E, I217L, L534V, L446F, P657K, I117L, P266L
- **Cell lines:** HEK293T — Homo sapiens (Human), Transformed cell line (CVCL_0063), pQE-80L — Oryctolagus cuniculus (Rabbit), Hybridoma (CVCL_N033), Escherichia coli BL21(DE3) — Mus musculus (Mouse), Hybridoma (CVCL_B7HM), pET-28a — Oryctolagus cuniculus (Rabbit), Transformed cell line (CVCL_6E94)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13010154/full.md

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Source: https://tomesphere.com/paper/PMC13010154