Nawaz Maryam, Huiyuan Yao, Akhtar Fahad, Tianyue Ma, Zheng Heng
School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211100, People's Republic of China.
Mol Divers. 2025 Mar 28. doi: 10.1007/s11030-025-11173-y.
Antiviral peptides (AVPs) represent a novel and promising therapeutic alternative to conventional antiviral treatments, due to their broad-spectrum activity, high specificity, and low toxicity. The emergence of zoonotic viruses such as Zika, Ebola, and SARS-CoV-2 have accelerated AVP research, driven by advancements in data availability and artificial intelligence (AI). This review focuses on the development of AVP databases, their physicochemical properties, and predictive tools utilizing machine learning for AVP discovery. Machine learning plays a pivotal role in advancing and developing antiviral peptides and peptidomimetics, particularly through the development of specialized databases such as DRAVP, AVPdb, and DBAASP. These resources facilitate AVP characterization but face limitations, including small datasets, incomplete annotations, and inadequate integration with multi-omics data.The antiviral efficacy of AVPs is closely linked to their physicochemical properties, such as hydrophobicity and amphipathic α-helical structures, which enable viral membrane disruption and specific target interactions. Computational prediction tools employing machine learning and deep learning have significantly advanced AVP discovery. However, challenges like overfitting, limited experimental validation, and a lack of mechanistic insights hinder clinical translation.Future advancements should focus on improved validation frameworks, integration of in vivo data, and the development of interpretable models to elucidate AVP mechanisms. Expanding predictive models to address multi-target interactions and incorporating complex biological environments will be crucial for translating AVPs into effective clinical therapies.
抗病毒肽(AVP)由于其广谱活性、高特异性和低毒性,成为传统抗病毒治疗的一种新颖且有前景的替代疗法。寨卡病毒、埃博拉病毒和严重急性呼吸综合征冠状病毒2(SARS-CoV-2)等人畜共患病毒的出现,在数据可获取性和人工智能(AI)进步的推动下,加速了AVP的研究。本综述重点关注AVP数据库的发展、其物理化学性质以及利用机器学习发现AVP的预测工具。机器学习在推进和开发抗病毒肽及肽模拟物方面发挥着关键作用,特别是通过开发诸如DRAVP、AVPdb和DBAASP等专门数据库。这些资源有助于AVP的表征,但面临一些局限性,包括数据集小、注释不完整以及与多组学数据整合不足。AVP的抗病毒功效与其物理化学性质密切相关,如疏水性和两亲性α-螺旋结构,这些性质能够破坏病毒膜并实现特定的靶标相互作用。采用机器学习和深度学习的计算预测工具显著推进了AVP的发现。然而,诸如过拟合、有限的实验验证以及缺乏机制性见解等挑战阻碍了其临床转化。未来的进展应侧重于改进验证框架、整合体内数据以及开发可解释模型以阐明AVP的作用机制。扩展预测模型以解决多靶标相互作用并纳入复杂的生物环境对于将AVP转化为有效的临床疗法至关重要。