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February 13, 2026Journal of the American Chemical Society3 citations

Cebulassopins, Antiproliferative Lasso Peptides from a Split Biosynthetic Operon

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SUSoohyun UmHJHyeongju JeongJGJack G. Ganley

Key Points

  • This study aims to characterize cebulassopins, a new class of lasso peptides, and evaluate their biological activity.
  • Characterization of structure and topology of cebulassopins A-D
  • Analysis of biosynthetic gene cluster arrangement
  • Evaluation of antiproliferative activity against human lung carcinoma cells
  • Cebulassopins A-D are identified as lasso peptides synthesized by a split operon
  • Both cebulassopins 1 and 2 exhibit sub-μM inhibitory concentrations against cancer cells
  • This discovery indicates a novel mechanism for lasso peptide synthesis

Abstract

Lasso peptides are a class of ribosomally synthesized and post-translationally modified peptides distinguished by their lasso-like, threaded topology. Common to all lasso peptides biosynthetic gene clusters examined so far is an arrangement whereby the precursor peptide is encoded adjacent to the macrolactam synthetase and other modification genes. Here we report the cebulassopins A-D (1-4), the first example of lasso peptides synthesized by a split operon whereby multiple precursors are encoded several Mbps distant from the modification enzymes. Aside from characterizing their structures and calculating the three-dimensional topology of 1 and 2, we also find that the cebulassopins are potent antiproliferative agents with sub-μM inhibitory concentrations against human lung carcinoma cells. These results set the stage for further biological examination and exploration of other split lasso peptide gene clusters.

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Cite This Study

Um et al. (2026) studied this question.

synapsesocial.com/papers/698ebf1d85a1ff6a93016504https://doi.org/10.1021/jacs.5c14658
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