Cebulassopins, Antiproliferative Lasso Peptides from a Split Biosynthetic Operon

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Authors: Soohyun Um, Hyeongju Jeong, Jack G. Ganley, Brett C. Covington, Sehwan Choi, C. Zhang, Wonkyung Kim, Mohammad R. Seyedsayamdost, Kyuho Moon
Cited by: 4
References: 31

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.

Fields of Study & Subjects

Microbial Natural Products and Biosynthesis Chemical Synthesis and Analysis Biochemical and Structural Characterization

Publication details

Journal / source
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Volume
148
Issue
7
Pages
6739–6743
Publication date
10 February 2026
Language
EN