TC-DTA: Predicting Drug-Target Binding Affinity With Transformer and Convolutional Neural Networks

卷积神经网络 计算机科学 药品 人工神经网络 变压器 人工智能 模式识别(心理学) 生物系统 材料科学 物理 药理学 医学 电压 生物 量子力学
作者
Xiwei Tang,Yiqiang Zhou,Mengyun Yang,Wenjun Li
出处
期刊:IEEE Transactions on Nanobioscience [Institute of Electrical and Electronics Engineers]
卷期号:23 (4): 572-578 被引量:12
标识
DOI:10.1109/tnb.2024.3441590
摘要

Bioinformatics is a rapidly evolving field that applies computational methods to analyze and interpret biological data. A key task in bioinformatics is identifying novel drug-target interactions (DTIs), which plays a crucial role in drug discovery. Most computational approaches treat DTI prediction as a binary classification problem, determining whether drug-target pairs interact. However, with the growing availability of drug-target binding affinity data, this binary task can be reframed as a regression problem focused on drug-target affinity (DTA). DTA quantifies the strength of drug-target binding, offering more detailed insights than DTI and serving as a valuable tool for virtual screening in drug discovery. Accurately predicting compound interactions with targets can accelerate the drug development process. In this study, we introduce a deep learning model named TC-DTA for DTA prediction, leveraging convolutional neural networks (CNN) and the encoder module of the transformer architecture. We begin by extracting raw drug SMILES strings and protein amino acid sequences from the dataset, which are then represented using various encoding methods. Subsequently, we employ CNN and the transformer's encoder module to extract features from the drug SMILES strings and protein sequences, respectively. Finally, the feature information is concatenated and input into a multi-layer perceptron to predict binding affinity scores. We evaluated our model on two benchmark DTA datasets, Davis and KIBA, comparing it with methods such as KronRLS, SimBoost, and DeepDTA. Our model, TC-DTA, outperformed these baseline methods based on evaluation metrics like Mean Squared Error (MSE), Concordance Index (CI), and Regression towards the Mean Index ( rm2 ). These results highlight the effectiveness of the Transformer's encoder and CNN in extracting meaningful representations from sequences, thereby enhancing DTA prediction accuracy. This deep learning model can accelerate drug discovery by identifying drug candidates with high binding affinity to specific targets. Compared to traditional methods, machine learning technology offers a more effective and efficient approach to drug discovery.
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
eternal_dreams完成签到 ,获得积分10
3秒前
今天晚上早点睡完成签到 ,获得积分10
6秒前
认真二娘11完成签到 ,获得积分10
8秒前
英姑应助冷言采纳,获得30
8秒前
文静灵阳完成签到 ,获得积分10
10秒前
稳重紫蓝完成签到 ,获得积分10
11秒前
耍酷的含羞草完成签到,获得积分20
14秒前
充电宝应助微S采纳,获得10
16秒前
18秒前
desperate完成签到,获得积分10
20秒前
牧林听风完成签到 ,获得积分10
20秒前
量子星尘发布了新的文献求助10
22秒前
深情安青应助niko采纳,获得10
25秒前
小马甲应助niko采纳,获得10
25秒前
烟花应助niko采纳,获得10
25秒前
25秒前
ding应助niko采纳,获得10
25秒前
JamesPei应助niko采纳,获得10
25秒前
顾矜应助niko采纳,获得10
25秒前
所所应助niko采纳,获得10
25秒前
在水一方应助niko采纳,获得10
25秒前
共享精神应助niko采纳,获得10
25秒前
小马甲应助niko采纳,获得10
25秒前
maxthon完成签到,获得积分10
27秒前
30秒前
微S发布了新的文献求助10
30秒前
洁净之玉发布了新的文献求助10
33秒前
34秒前
夏知许完成签到 ,获得积分10
36秒前
周琦发布了新的文献求助10
38秒前
Shuhe_Gong完成签到 ,获得积分10
38秒前
量子星尘发布了新的文献求助10
39秒前
44秒前
44秒前
45秒前
45秒前
45秒前
mmd完成签到 ,获得积分10
47秒前
47秒前
47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
Aerospace Standards Index - 2026 ASIN2026 3000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Social Work and Social Welfare: An Invitation(7th Edition) 410
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 6051321
求助须知:如何正确求助?哪些是违规求助? 7859022
关于积分的说明 16267625
捐赠科研通 5196359
什么是DOI,文献DOI怎么找? 2780596
邀请新用户注册赠送积分活动 1763538
关于科研通互助平台的介绍 1645561