DeepB3P:基于转换器的血脑屏障穿透肽识别模型,使用反馈 GAN 进行数据扩增。

Qiang Tang, Wei Chen
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引用次数: 0

摘要

简介血脑屏障(BBB)是一道关键的结构屏障,阻碍了大多数神经治疗药物进入大脑。这给中枢神经系统(CNS)药物的开发带来了巨大挑战,因为目前缺乏有效的给药技术来克服这一障碍。BBB 穿透肽(BBBPs)有望克服 BBB,促进药物分子进入大脑。因此,精确鉴定 BBBPs 已成为中枢神经系统药物开发的关键步骤。然而,大多数计算方法都是基于传统模型设计的,无法充分捕捉到 BBBPs 与 BBB 之间错综复杂的相互作用。此外,不平衡数据集也进一步影响了这些方法的性能:本研究解决了 BBBP 预测中不平衡数据集的问题,并提出了一种强大的预测方法,可高效、准确地识别 BBBPs,并生成类似的 BBBPs:方法:提出了一种基于变换器的深度学习模型 DeepB3P,用于预测 BBBP。采用反馈生成对抗网络(FBGAN)模型有效生成类比 BBBP,解决数据不平衡问题:结果:FBGAN模型有能力生成新颖的类BBBP肽,有效缓解了BBBP预测中的数据不平衡问题。在基准数据集上进行的大量实验表明,DeepB3P的特异性、准确性和马修相关系数分别比其他BBBP预测模型高出约9.09%、4.55%和9.41%。为了加快BBBP鉴定和中枢神经系统药物设计的进展,DeepB3P以网络服务器的形式实现,可在http://cbcb.cdutcm.edu.cn/deepb3p/.Conclusion:DeepB3P 提供的可解释分析为 BBBP 鉴定提供了有价值的见解并加强了下游分析。此外,FBGAN 生成的 BBBP 类似肽具有开发中枢神经系统药物的潜力。
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DeepB3P: A transformer-based model for identifying blood-brain barrier penetrating peptides with data augmentation using feedback GAN.

Introduction: The blood-brain barrier (BBB) serves as a critical structural barrier and impedes the entry of most neurotherapeutic drugs into the brain. This poses substantial challenges for central nervous system (CNS) drug development, as there is a lack of efficient drug delivery technologies to overcome this obstacle. BBB penetrating peptides (BBBPs) hold promise in overcoming the BBB and facilitating the delivery of drug molecules to the brain. Therefore, precise identification of BBBPs has become a crucial step in CNS drug development. However, most computational methods are designed based on conventional models that inadequately capture the intricate interaction between BBBPs and the BBB. Moreover, the performance of these methods was further hampered by unbalanced datasets.

Objectives: This study addresses the problem of unbalanced datasets in BBBP prediction and proposes a powerful predictor for efficiently and accurately identifying BBBPs, as well as generating analogous BBBPs.

Methods: A transformer-based deep learning model, DeepB3P, was proposed for predicting BBBP. The feedback generative adversarial network (FBGAN) model was employed to effectively generate analogous BBBPs, addressing data imbalance.

Results: The FBGAN model possesses the ability to generate novel BBBP-like peptides, effectively mitigating the data imbalance in BBBP prediction. Extensive experiments on benchmarking datasets demonstrated that DeepB3P outperforms other BBBP prediction models by approximately 9.09%, 4.55% and 9.41% in terms of specificity, accuracy, and Matthew's correlation coefficient, respectively. For accelerating the progress in BBBP identification and CNS drug design, the proposed DeepB3P was implemented as a webserver, which is accessible at http://cbcb.cdutcm.edu.cn/deepb3p/.

Conclusion: The interpretable analyses provided by DeepB3P offer valuable insights and enhance downstream analyses for BBBP identification. Moreover, the BBBP-like peptides generated by FBGAN hold potential as candidates for CNS drug development.

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