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.
Authors
- Susanna E. Barrett (ORCID: https://orcid.org/0000-0003-3149-6654)
- Douglas A. Mitchell (ORCID: https://orcid.org/0000-0002-9564-0953)
- Diwakar Shukla (ORCID: https://orcid.org/0000-0003-4079-5381)
- Xuenan Mi (ORCID: https://orcid.org/0009-0001-5237-4712)
Institutions
- University of Illinois Urbana-Champaign (US)
- Vanderbilt University (US)
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
Funders
- National Science Foundation
- National Institutes of Health
- University of Illinois at Urbana-Champaign