Liu Xianliang, Luo Jiawei, Wang Xinyan, Zhang Yang, Chen Junjie
School of Computer Science and Technology, Harbin Institute of Technology, HIT Campus, Shenzhen University Town, Nanshan District, Shenzhen 518055, Guangdong, China.
Core Research Facility, Southern University of Science and Technology, No. 1088 Xueyuan Road, Nanshan District, Shenzhen 518055, Guangdong, China.
Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbae715.
Antimicrobial peptides (AMPs) emerge as a type of promising therapeutic compounds that exhibit broad spectrum antimicrobial activity with high specificity and good tolerability. Natural AMPs usually need further rational design for improving antimicrobial activity and decreasing toxicity to human cells. Although several algorithms have been developed to optimize AMPs with desired properties, they explored the variations of AMPs in a discrete amino acid sequence space, usually suffering from low efficiency, lack diversity, and local optimum. In this work, we propose a novel directed evolution method, named PepZOO, for optimizing multi-properties of AMPs in a continuous representation space guided by multi-objective zeroth-order optimization. PepZOO projects AMPs from a discrete amino acid sequence space into continuous latent representation space by a variational autoencoder. Subsequently, the latent embeddings of prototype AMPs are taken as start points and iteratively updated according to the guidance of multi-objective zeroth-order optimization. Experimental results demonstrate PepZOO outperforms state-of-the-art methods on improving the multi-properties in terms of antimicrobial function, activity, toxicity, and binding affinity to the targets. Molecular docking and molecular dynamics simulations are further employed to validate the effectiveness of our method. Moreover, PepZOO can reveal important motifs which are required to maintain a particular property during the evolution by aligning the evolutionary sequences. PepZOO provides a novel research paradigm that optimizes AMPs by exploring property change instead of exploring sequence mutations, accelerating the discovery of potential therapeutic peptides.
抗菌肽(AMPs)作为一类有前景的治疗性化合物出现,具有广谱抗菌活性、高特异性和良好的耐受性。天然抗菌肽通常需要进一步合理设计,以提高抗菌活性并降低对人体细胞的毒性。尽管已经开发了几种算法来优化具有所需特性的抗菌肽,但它们在离散的氨基酸序列空间中探索抗菌肽的变异,通常效率低下、缺乏多样性且存在局部最优问题。在这项工作中,我们提出了一种名为PepZOO的新型定向进化方法,用于在多目标零阶优化的引导下,在连续表示空间中优化抗菌肽的多种特性。PepZOO通过变分自编码器将抗菌肽从离散的氨基酸序列空间投影到连续的潜在表示空间。随后,将原型抗菌肽的潜在嵌入作为起点,并根据多目标零阶优化的指导进行迭代更新。实验结果表明,在改善抗菌功能、活性、毒性以及与靶点的结合亲和力等多种特性方面,PepZOO优于现有方法。进一步采用分子对接和分子动力学模拟来验证我们方法的有效性。此外,PepZOO可以通过比对进化序列揭示在进化过程中维持特定特性所需的重要基序。PepZOO提供了一种新的研究范式,即通过探索特性变化而非序列突变来优化抗菌肽,加速了潜在治疗性肽的发现。