LassoESM a tailored language model for enhanced lasso peptide property prediction

Ribosomally synthesized and post-translationally modified peptides (RiPPs) are a diverse group of natural products. The lasso peptide class of RiPPs adopt a unique [1]rotaxane conformation formed by a lasso cyclase, conferring diverse bioactivities and remarkable stability. The prediction of lasso peptide properties, such as substrate compatibility with a particular lasso cyclase or desired biological activity, remains challenging due to limited experimental data and the complexity of substrate fitness landscapes. Here, we develop LassoESM, a tailored language model that improves lasso peptide property prediction. LassoESM embeddings enable accurate prediction of substrate compatibility, facilitate identification of novel non-cognate cyclase-substrate pairs, and enhance prediction of RNA polymerase inhibitory activity, a biological activity of several known lasso peptides. We anticipate that LassoESM and future iterations will be instrumental in the rational design and discovery of lasso peptides with tailored functions.

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Publication Details

Journal
Nature Communications
Published
2025-09-29
DOI
https://doi.org/10.1038/s41467-025-63412-3
Citations
3
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
2.42

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article

LassoESM a tailored language model for enhanced lasso peptide property prediction

Susanna E. Barrett, Douglas A. Mitchell, Diwakar Shukla, Xuenan Mi
3 citations
Nature Communications
Chemical Synthesis and Analysis
2.42
article

LassoESM a tailored language model for enhanced lasso peptide property prediction

Susanna E. Barrett, Douglas A. Mitchell, Diwakar Shukla, Xuenan Mi
article en
3 citations

Abstract

Ribosomally synthesized and post-translationally modified peptides (RiPPs) are a diverse group of natural products. The lasso peptide class of RiPPs adopt a unique [1]rotaxane conformation formed by a lasso cyclase, conferring diverse bioactivities and remarkable stability. The prediction of lasso peptide properties, such as substrate compatibility with a particular lasso cyclase or desired biological activity, remains challenging due to limited experimental data and the complexity of substrate fitness landscapes. Here, we develop LassoESM, a tailored language model that improves lasso peptide property prediction. LassoESM embeddings enable accurate prediction of substrate compatibility, facilitate identification of novel non-cognate cyclase-substrate pairs, and enhance prediction of RNA polymerase inhibitory activity, a biological activity of several known lasso peptides. We anticipate that LassoESM and future iterations will be instrumental in the rational design and discovery of lasso peptides with tailored functions.

Nature CommunicationsVol. 16(1)
University of Illinois Urbana-Champaign (US), Vanderbilt University (US)
National Science Foundation, National Institutes of Health, University of Illinois at Urbana-Champaign
Openalex Percentile: Top 10%
Chemical Synthesis and Analysis
2.42
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