A conditional denoising VAE-based framework for antimicrobial peptides generation with preserving desirable properties.

Weizhong Zhao, Kaijieyi Hou, Yiting Shen, Xiaohua Hu
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Abstract

Motivation: The widespread use of antibiotics has led to the emergence of resistant pathogens. Antimicrobial peptides (AMPs) combat bacterial infections by disrupting the integrity of cell membranes, making it challenging for bacteria to develop resistance. Consequently, AMPs offer a promising solution to addressing antibiotic resistance. However, the limited availability of natural AMPs cannot meet the growing demand. While deep learning technologies have advanced AMP generation, conventional models often lack stability and may introduce unforeseen side effects.

Results: This study presents a novel denoising VAE-based model guided by desirable physicochemical properties for AMP generation. The model integrates key features (e.g. molecular weight, isoelectric point, hydrophobicity, etc.), and employs position encoding along with a Transformer architecture to enhance generation accuracy. A customized loss function, combining reconstruction loss, KL divergence, and property preserving loss ensure effective model training. Additionally, the model incorporates a denoising mechanism, enabling it to learn from perturbed inputs, thus maintaining performance under limited training data. Experimental results demonstrate that the proposed model can generate AMPs with desirable functional properties, offering a viable approach for AMP design and analysis, which ultimately contributes to the fight against antibiotic resistance.

Availability and implementation: The data and source codes are available both in GitHub (https://github.com/David-WZhao/PPGC-DVAE) and Zenodo (DOI 10.5281/zenodo.14730711).

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一种条件去噪的基于vae的抗菌肽生成框架。
动机:抗生素的广泛使用导致了耐药病原体的出现。抗菌肽(AMPs)通过破坏细胞膜的完整性来对抗细菌感染,使细菌难以产生耐药性。因此,amp为解决抗生素耐药性提供了一个有希望的解决方案。然而,天然抗菌肽的有限供应无法满足日益增长的需求。虽然深度学习技术具有先进的AMP生成技术,但传统模型往往缺乏稳定性,并可能引入不可预见的副作用。结果:本研究提出了一种新的基于vae的去噪模型,该模型以理想的物理化学性质为指导,用于生成amp。该模型集成了关键特征(如分子量、等电点、疏水性等),并采用位置编码和Transformer架构来提高生成精度。定制的损失函数结合了重建损失、KL散度和财产保留损失,确保了有效的模型训练。此外,该模型结合了去噪机制,使其能够从扰动输入中学习,从而在有限的训练数据下保持性能。实验结果表明,该模型可以生成具有理想功能特性的抗菌肽,为抗菌肽的设计和分析提供了一种可行的方法,最终有助于对抗抗生素耐药性。可用性和实现:数据和源代码都可以在GitHub (https://github.com/David-WZhao/PPGC-DVAE)和Zenodo (DOI 10.5281/ Zenodo .14730711)中获得。联系方式和补充信息:wzzhao@ccnu.edu.cn,补充材料可在Bioinformatics在线获取。
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