PepBAN: A Deep Learning Framework with Bilinear Attention and Adversarial Learning for Peptide–Protein Interaction Prediction

对抗制 深度学习 人工智能 计算机科学 图形 一般化 机器学习 水准点(测量) 理论计算机科学 数学 大地测量学 数学分析 地理
作者
Shizhuo Li,Xiaorui Wang,Yuchen Zhu,Jingxuan Ge,Donghai Zhao,Hongxia Xu,Tingjun Hou,Chang‐Yu Hsieh
出处
期刊:Journal of Chemical Information and Modeling [American Chemical Society]
卷期号:65 (17): 9061-9074
标识
DOI:10.1021/acs.jcim.5c01713
摘要

Accurate prediction of the peptide-protein interaction (PepPI) is crucial for developing peptide-based therapeutics and vaccines. However, this computational task has traditionally faced significant challenges, such as the scarcity of structure data along with the corresponding label of the binding affinity for bound complexes. To address these challenges, we introduce PepBAN, a deep learning framework for modeling PepPI predictions. PepBAN incorporates two technical advancements: (1) adopting the protein language model ESM-2 to characterize proteins and ESM-2 or a graph-based foundation model for peptides without structure data and (2) leveraging the conditional domain adversarial learning to enhance generalization across a broad range of protein targets, especially when there are limited binding data. At the core of PepBAN is a bilinear attention network (BAN) that effectively learns the pattern of pairwise local interactions, enables the identification of key residues participating in the peptide-protein interactions, and offers an intuitive approach to interpret the underlying mechanisms of PepPIs via analyzing attention weights. Our numerical experiments demonstrated that PepBAN outperformed the previous state-of-the-art models across several well-established benchmark studies. Furthermore, we evaluated PepBAN's applicability in predicting cyclic peptide-protein interactions, a task that poses significant challenges due to the presence of noncanonical amino acids. These nonstandard residues require specialized handling, which most existing sequence-based PepPI prediction models did not adequately address, and we adopt an atom-resolved molecular graph approach to process cyclic peptides. Despite this complexity, PepBAN demonstrated a clear advantage by achieving a superior prediction performance and offering a distinct edge in tackling the emerging chemical space of cyclic peptides, which has great potential for novel therapeutic development. In summary, PepBAN serves as a valuable tool for advancing peptide-based drug and therapeutic development.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI6.3应助赵明月采纳,获得10
1秒前
1秒前
Matberry完成签到 ,获得积分10
1秒前
fairy完成签到 ,获得积分10
2秒前
zcz发布了新的文献求助50
3秒前
万能图书馆应助鄂闽工贸采纳,获得10
3秒前
qqqq11发布了新的文献求助10
4秒前
李爱国应助Serendipity采纳,获得10
4秒前
拼搏尔蓝发布了新的文献求助10
5秒前
5秒前
曹能豪发布了新的文献求助10
5秒前
和谐妙柏发布了新的文献求助30
5秒前
5秒前
科研NIU应助xiaotian采纳,获得10
6秒前
6秒前
7秒前
乐空思应助kingwill采纳,获得50
7秒前
bkagyin应助Chur采纳,获得10
7秒前
斯文败类应助零柒采纳,获得10
7秒前
7秒前
赘婿应助激情的小蝴蝶采纳,获得10
8秒前
万能图书馆应助lcj采纳,获得10
8秒前
样样精通完成签到,获得积分10
8秒前
st完成签到,获得积分10
9秒前
10秒前
顾矜应助XYN1采纳,获得10
10秒前
10秒前
小z完成签到,获得积分10
10秒前
xin发布了新的文献求助10
10秒前
10秒前
11秒前
科研通AI6.3应助abcc1234采纳,获得30
11秒前
过几天发布了新的文献求助10
11秒前
11秒前
11秒前
孙成发布了新的文献求助10
12秒前
小z发布了新的文献求助10
13秒前
华仔应助黑马王子采纳,获得10
14秒前
白落落发布了新的文献求助10
15秒前
JeromineJade完成签到,获得积分10
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Principles of town planning : translating concepts to applications 500
Modified letrozole versus GnRH antagonist protocols in ovarian aging women for IVF: An Open-Label, Multicenter, Randomized Controlled Trial 360
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6063292
求助须知:如何正确求助?哪些是违规求助? 7895855
关于积分的说明 16314576
捐赠科研通 5206720
什么是DOI,文献DOI怎么找? 2785451
邀请新用户注册赠送积分活动 1768084
关于科研通互助平台的介绍 1647500