A deep learning framework (CreoPep) for target-specific design and optimization of conotoxin peptides
Cheng Ge1,2, Han-Shen Tae3, Lu Lu1,2
1Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.
None:
Conotoxins are small, disulfide-rich peptides that display exceptional affinity and selectivity for ion channels and receptors, making them valuable templates for therapeutic development. However, their optimization remains challenging due to the limited diversity of naturally occurring variants and the labor-intensive nature of conventional engineering strategies. Here, we present CreoPep, a deep learning-based generative framework specifically developed to design and optimize conotoxins targeting defined receptors. CreoPep integrates masked language modeling with a progressive masking scheme and employs an augmentation pipeline that combines physics-based energy screening with temperature-controlled multinomial sampling. This enables the generation of structurally and functionally diverse peptide variants while retaining essential pharmacological features. Structural analysis shows that CreoPep-generated variants adopt both conserved and previously unobserved binding modes, including disulfide-deficient forms. Together, these findings establish CreoPep as a powerful computational-experimental framework for the rational design of conotoxin-based peptides and provide a foundation for extending similar approaches to other peptide families.
More Related Videos
05:50Pharmacophore Modeling for Targets with Extensive Ligand Libraries: A Case Study on SARS-CoV-2 Mpro
Published on: September 26, 2025
06:50Author Spotlight: A Computational Approach to Decipher Amino Acid Preferences in Multispecific Protein-Protein Interactions
Published on: January 26, 2024
Related Concept Videos
Conservative Site-specific Recombination and Phase Variation
The recognition sites for Cre recombinase called LoxP...
Conserved Binding Sites
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
