Papers › Accelerating Antimicrobial Peptide Discovery with Latent Structure

Accelerating Antimicrobial Peptide Discovery with Latent Structure

28 Nov 2022arXiv:2212.09450archive 2025-07-28

Danqing Wang, Zeyu Wen, Fei Ye, Lei LI, Hao Zhou

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.

PaperPDFCode

In Syntology Open this paper in Syntology's Atlas, the map of the papers in Syntology's graph and their citations.

Code

dqwang122/lssamp officialmentioned in paperpytorch report

Repository list and official/mentioned flags are the archive's, frozen 2025-07-28. Reachability, where shown, is from one Syntology probe window (2026-09-16 to 2026-09-18); repositories not probed show nothing. GitHub stars are not tracked.

Code Syntology ran Syntology

Not run by Syntology. Nothing on this page verifies that the listed code works.

Tasks

Quantization

Results from the paper archive 2025-07-28

No leaderboard rows for this paper in the archive.

Methods

AMPVQ-VAE

Report a problem or propose a change · a person checks every report against the paper or source before anything changes; decisions are listed on /corrections