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Accelerating Antimicrobial Peptide Discovery with Latent Structure
November 28, 2022 Β· Entered Twilight Β· π Knowledge Discovery and Data Mining
Repo contents: .gitignore, README.md, baseline.sh, configs, data, finetune.sh, requirements.txt, run.sh, sample.sh, src
Authors
Danqing Wang, Zeyu Wen, Fei Ye, Lei Li, Hao Zhou
arXiv ID
2212.09450
Category
q-bio.BM
Cross-listed
cs.CE,
cs.LG
Citations
7
Venue
Knowledge Discovery and Data Mining
Repository
https://github.com/dqwang122/LSSAMP
β 12
Last Checked
2 months ago
Abstract
Antimicrobial peptides (AMPs) are promising therapeutic approaches against drug-resistant pathogens. Recently, deep generative models are used to discover new AMPs. However, previous studies mainly focus on peptide sequence attributes and do not consider crucial structure information. In this paper, we propose a latent sequence-structure model for designing AMPs (LSSAMP). LSSAMP exploits multi-scale vector quantization in the latent space to represent secondary structures (e.g. alpha helix and beta sheet). By sampling in the latent space, LSSAMP can simultaneously generate peptides with ideal sequence attributes and secondary structures. Experimental results show that the peptides generated by LSSAMP have a high probability of antimicrobial activity. Our wet laboratory experiments verified that two of the 21 candidates exhibit strong antimicrobial activity. The code is released at https://github.com/dqwang122/LSSAMP.
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