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Generating Antimicrobial Peptides from Latent Secondary Structure Space

2021-09-29 · Danqing Wang, Zeyu Wen, Lei LI, Hao Zhou

Antimicrobial peptides (AMPs) have shown promising results in broad-spectrum antibiotics and resistant infection treatments, which makes it attract plenty of attention in drug discovery. Recently, many researchers bring deep generative models to AMP design. However, few studies consider structure information during the generation, though it has shown crucial influence on antimicrobial activity in all AMP mechanism theories. In this paper, we propose LSSAMP that uses the multi-scale VQ-VAE to learn the positional latent spaces modeling the secondary structure. By sampling in the latent secondary structure space, we can generate peptides with ideal amino acids and secondary structures at the same time. Experimental results show that our LSSAMP can generate peptides with multiply ideal physical attributes and a high probability of being predicted as AMPs by public AMP prediction models.

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Drug Discovery

Methods 이 논문이 사용한 방법론

VQ-VAE VQ-VAE is a type of variational autoencoder that uses vector quantisation to obtain a discrete latent representation. It differs from…
AMP Based on the understanding that the flat local minima of the empirical risk cause the model to generalize better. Adversarial Model Perturbation (AMP) improves generalization via…

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