AntiFlamPred: An Anti-Inflammatory Peptide Predictor for Drug Selection Strategies

被引:7
作者
Alotaibi, Fahad [1 ]
Attique, Muhammad [2 ,3 ]
Khan, Yaser Daanial [2 ]
机构
[1] King Abdulaziz Univ, Fac Comp & Informat Technol, Dept Informat Syst, Jeddah 21589, Saudi Arabia
[2] Univ Management & Technol, Dept Comp Sci, Lahore 54000, Pakistan
[3] Univ Gujrat, Dept Informat Technol, Gujrat 50700, Pakistan
来源
CMC-COMPUTERS MATERIALS & CONTINUA | 2021年 / 69卷 / 01期
关键词
Prediction; feature extraction; machine learning; bootstrap aggregation; deep learning; bioinformatics; computational intelligence; anti-inflammatory peptides; VASOACTIVE-INTESTINAL-PEPTIDE; AUTOIMMUNE; DISEASE; INFLAMMATION; ROLES; THERAPY; DEFENSE; MODES;
D O I
10.32604/cmc.2021.017297
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Several autoimmune ailments and inflammation-related diseases emphasize the need for peptide-based therapeutics for their treatment and established substantial consideration. Though, the wet-lab experiments for the investigation of anti-inflammatory proteins/peptides ("AIP") are usually very costly and remain time-consuming. Therefore, before wet-lab investigations, it is essential to develop in-silico identification models to classify prospective anti-inflammatory candidates for the facilitation of the drug development process. Several anti-inflammatory prediction tools have been proposed in the recent past, yet, there is a space to induce enhancement in prediction performance in terms of precision and efficiency. An exceedingly accurate antiinflammatory prediction model is proposed, named AntiFlamPred ("Antiinflammatory Peptide Predictor"), by incorporation of encoded features and probing machine learning algorithms including deep learning. The proposed model performs best in conjunction with deep learning. Rigorous testing and validation were applied including cross-validation, self-consistency, jackknife, and independent set testing. The proposed model yielded 0.919 value for area under the curve (AUC) and revealed Mathew's correlation coefficient (MCC) equivalent to 0.735 demonstrating its effectiveness and stability. Subsequently, the proposed model was also extensively probed in comparison with other existing models. The performance of the proposed model also out-performs other existing models. These outcomes establish that the proposed model is a robust predictor for identifying AIPs and may subsidize well in the extensive lab-based examinations. Subsequently, it has the potential to assiduously support medical and bioinformatics research.
引用
收藏
页码:1039 / 1055
页数:17
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