Department of Computer Science, School of Systems and Technology, University of Management and Technology, Lahore-54770, Pakistan.
Brief Bioinform. 2022 Jan 17;23(1). doi: 10.1093/bib/bbab487.
Short antimicrobial peptides (sAMPs) belong to a significant repertoire of antimicrobial agents and are known to possess enhanced antimicrobial activity, higher stability and less toxicity to human cells, as well as less complex than other large biological drugs. As these molecules are significantly important, herein, a prediction method for sAMPs (with a sequence length ≤ 30 residues) is proposed for accurate and efficient prediction of sAMPs instead of laborious and costly experimental approaches. Benchmark dataset was collected from a recently reported study and sequences were converted into three channel images comprising information related to the position, frequency and sum of 12 physiochemical features as the first, second and third channels, respectively. Two image-based deep neural networks (DNNs), i.e. RESNET-50 and VGG-16 were trained and evaluated using various metrics while a comparative analysis with previous techniques was also performed. Validation of sAMP-PFPDeep was also performed by using molecular docking based analysis. The results showed that VGG-16 provided more accurate results, i.e. 98.30% training accuracy and 87.37% testing accuracy for predicting sAMPs as compared to those of RESNET-50 having 96.14% training accuracy and 83.87% testing accuracy. However, the comparative analysis revealed that both these models outperformed previously reported state-of-the-art methods. Based on the results, it is concluded that sAMP-PFPDeep can help identify antimicrobial peptides with promising accuracy and efficiency. It can help biologists and scientists to identify antimicrobial peptides, by further aiding the computer-aided drug design and discovery, as well as virtual screening protocols against various pathologies. sAMP-PFPDeep is available at (https://github.com/WaqarHusain/sAMP-PFPDeep).
短抗菌肽(sAMPs)属于一类重要的抗菌剂,具有增强的抗菌活性、更高的稳定性和对人体细胞的毒性较小,以及比其他大型生物药物更简单的特点。由于这些分子非常重要,因此,本文提出了一种 sAMPs 的预测方法(序列长度≤30 个残基),用于准确高效地预测 sAMPs,而不是采用繁琐且昂贵的实验方法。基准数据集是从最近的一项研究中收集的,序列被转换为三通道图像,其中包含与位置、频率和 12 种物理化学特征的总和相关的信息,分别作为第一、第二和第三通道。使用各种指标对两种基于图像的深度学习神经网络(DNN),即 RESNET-50 和 VGG-16 进行了训练和评估,同时还与以前的技术进行了比较分析。还通过基于分子对接的分析对 sAMP-PFPDeep 进行了验证。结果表明,VGG-16 提供了更准确的结果,即 98.30%的训练准确率和 87.37%的测试准确率,用于预测 sAMPs,而 RESNET-50 的训练准确率为 96.14%,测试准确率为 83.87%。然而,比较分析表明,这两种模型都优于以前报道的最先进的方法。基于这些结果,可以得出结论,sAMP-PFPDeep 可以帮助以有希望的准确性和效率识别抗菌肽。它可以帮助生物学家和科学家识别抗菌肽,通过进一步辅助计算机辅助药物设计和发现,以及针对各种病理的虚拟筛选协议。sAMP-PFPDeep 可在 (https://github.com/WaqarHusain/sAMP-PFPDeep) 获得。