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Abstract

The design of functional enzymes holds promise for transformative solutions across various domains but presents significant challenges. Inspired by the success of language models in generating nature-like proteins, we explored the potential of an enzyme-specific language model in designing catalytically active artificial enzymes. Here, we introduce ZymCTRL (enzyme control), a conditional language model trained on the enzyme sequence space, capable of generating enzymes based on user-defined specifications. Experimental validation at diverse data regimes and for different enzyme families demonstrated ZymCTRLs ability to generate active enzymes across various sequence identity ranges. Specifically, we describe the design of carbonic anhydrases and lactate dehydrogenases in zero-shot, without requiring further training of the model, and showcasing activity at sequence identities below 40% compared to natural proteins. Biophysical analysis confirmed the globularity and well-folded nature of the generated sequences. Furthermore, fine-tuning the model enabled the generation of lactate dehydrogenases outside of natural sequence space but with activity comparable to their natural counterparts. Two of the artificial lactate dehydrogenases were selected for scale production and successfully lyophilised, maintaining activity and demonstrating preliminary conversion in one-pot enzymatic cascades under extreme conditions. Our findings open a new door towards the rapid and cost-effective design of artificial proficient enzymes. The model and dataset are freely available to the community.

Abstract summary

Claude Opus 5.5 · xhigh effort · 18 Oct 2026 · from the abstract · CC BY-NC-ND 4.0

An enzyme-specific conditional language model generates active carbonic anhydrases and lactate dehydrogenases to user specification, some under 40% identity to natural proteins, with no retraining.

Language models have been successful at generating nature-like proteins, which is not the same as producing enzymes that catalyse a requested reaction. ZymCTRL conditions generation on user-defined specifications, and the authors back it with wet-lab activity both zero-shot and after fine-tuning.

Key results

  1. SuggestedWithout any further training, the model produced catalytically active designs in two enzyme families, including sequences far from anything natural.

    Carbonic anhydrases and lactate dehydrogenases generated zero-shot showed activity at sequence identities under 40% relative to natural proteins; biophysical analysis indicated the generated sequences were globular and well folded. No kinetic values are reported. · Abstract

  2. SuggestedFine-tuning pushed designs outside natural sequence space while keeping activity at natural levels.

    Fine-tuned generation yielded lactate dehydrogenases described as lying outside natural sequence space with activity comparable to their natural counterparts; the comparison is stated without measurements. · Abstract

  3. SuggestedTwo designed dehydrogenases survived production and formulation well enough for a first process test.

    Both were taken to scale production and lyophilised, kept activity afterwards, and gave preliminary conversion in one-pot enzymatic cascades run under extreme conditions; the conditions and conversion levels are not specified. · Abstract

Methods, data and reproducibility

ZymCTRL is a conditional language model trained on enzyme sequence space that emits sequences for user-defined specifications. Carbonic anhydrase and lactate dehydrogenase designs were generated zero-shot and, for the dehydrogenases, after fine-tuning, then experimentally tested for catalytic activity, with biophysical checks on folding plus scale-up, lyophilisation and cascade testing for two designs.

  • Enzyme sequence space used to train the conditional language model
  • Generated carbonic anhydrases and lactate dehydrogenases taken through experimental validation · n = two artificial lactate dehydrogenases taken to scale production
Methods & tools
ZymCTRL
Reproducibility gaps
The model and dataset are stated to be freely available to the community, but no URL, repository or accession is printed in the text.
Limitations (2)
  • No activity measurements appear in the abstract: claims such as activity comparable to natural enzymes come without kinetic constants, expression yields, or the number of designs assayed. · noted in this summary
  • Validation covers two enzyme families, and the hit rate (how many generated sequences had to be screened per active one) is not reported, so design efficiency cannot be assessed. · noted in this summary

Read this if you design enzymes or assess protein language models, and want a case where conditional generation was carried through expression, activity assays and scale-up.

Citations
47

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