De novo Folding Mechanisms of Lasso Peptides

model. Additionally, the substantial entropy cost opposed lasso peptide folding. Simulations mimicking enzymatic spatial confinement reduced this penalty and stabilize folding. Leveraging Variational AutoEncoder-based pathway clustering, we resolved distinct pathway channels and representative folding pathways. Together, these findings establish representative folding models and fundamental thermodynamic and kinetic principles for rational engineering of lasso peptides.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-04-01
DOI
https://doi.org/10.64898/2026.03.30.715466
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
0.00

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article

De novo Folding Mechanisms of Lasso Peptides

Susanna E. Barrett, D. P. Mitchell, Diwakar Shukla, Xuenan Mi et al.
bioRxiv (Cold Spring Harbor Laboratory)
Biochemical and Structural Characterization
article

De novo Folding Mechanisms of Lasso Peptides

Susanna E. Barrett, D. P. Mitchell, Diwakar Shukla, Xuenan Mi, Song Yin
article en

Abstract

model. Additionally, the substantial entropy cost opposed lasso peptide folding. Simulations mimicking enzymatic spatial confinement reduced this penalty and stabilize folding. Leveraging Variational AutoEncoder-based pathway clustering, we resolved distinct pathway channels and representative folding pathways. Together, these findings establish representative folding models and fundamental thermodynamic and kinetic principles for rational engineering of lasso peptides.

bioRxiv (Cold Spring Harbor Laboratory)
University of Illinois Urbana-Champaign (US), Vanderbilt University (US)
National Institutes of Health
Openalex Percentile: Top 30%
Biochemical and Structural Characterization
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