ESM2_AMP: an interpretable framework for protein–protein interactions prediction and biological mechanism discovery

机制(生物学) 计算机科学 计算生物学 蛋白质-蛋白质相互作用 人工智能 生物 生物化学 物理 量子力学
作者
Yawen Sun,Rui Wang,Zeyu Luo,Lijun Tan,Junhao Liu,Ruimeng Li,Dong‐Qing Wei,Yu‐Juan Zhang
出处
期刊:Briefings in Bioinformatics [Oxford University Press]
卷期号:26 (4)
标识
DOI:10.1093/bib/bbaf434
摘要

The prediction of binary protein-protein interactions (PPIs) is essential for protein engineering, but a major challenge in deep learning-based methods is the unknown decision-making process of the model. To address this challenge, we propose the ESM2_AMP framework, which utilizes the ESM2 protein language model for extracting segment features from actual amino acid sequences and integrates the Transformer model for feature fusion in binary PPIs prediction. Further, the two distinct models, ESM2_AMPS and ESM2_AMP_CSE are developed to systematically explore the contributions of segment features and combine with special tokens features in the decision-making process. The experimental results reveal that the model relying on segment features demonstrates strong correlations between segments with high attention weights and known functional regions of amino acid sequences. This insight suggests that attention to these segments helps capture biologically relevant functional and interaction-related information. By analyzing the coverage relationship between high-attention sequence fragments and functional regions, we validated the model's ability to capture key segment features of PPIs and revealed the critical role of functional domains in PPIs. This finding not only enhances the interpretability methods for sequence-based prediction models but also provides biological evidence supporting the important regulatory role of functional sequences in protein-protein interactions. It offers cross-disciplinary insights for algorithm optimization and experimental validation research in the field of computational biology.
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
dde应助科研通管家采纳,获得10
1秒前
Nole应助科研通管家采纳,获得10
1秒前
Xxx完成签到,获得积分10
1秒前
Owen应助科研通管家采纳,获得10
1秒前
1秒前
初景应助明亮沂采纳,获得20
1秒前
1秒前
Nole应助科研通管家采纳,获得10
1秒前
Lucas应助科研通管家采纳,获得10
2秒前
英俊的铭应助科研通管家采纳,获得10
2秒前
田様应助科研通管家采纳,获得10
2秒前
2秒前
2秒前
2秒前
领导范儿应助科研通管家采纳,获得10
2秒前
3秒前
丘比特应助科研通管家采纳,获得10
3秒前
科研通AI6.2应助Leo采纳,获得30
3秒前
Nole应助科研通管家采纳,获得10
3秒前
王瑞完成签到 ,获得积分10
4秒前
小蘑菇应助蔡宇滔采纳,获得10
5秒前
6秒前
俭朴完成签到,获得积分20
6秒前
kktwo应助千贝儿采纳,获得10
6秒前
小二郎应助Longfenzhong采纳,获得10
8秒前
顺顺过过完成签到 ,获得积分10
8秒前
10秒前
栗早完成签到 ,获得积分10
11秒前
11秒前
共享精神应助欣喜采纳,获得10
12秒前
科研通AI6.2应助云贝采纳,获得10
12秒前
大意的小丸子完成签到 ,获得积分10
12秒前
CHEN发布了新的文献求助10
15秒前
离个大谱发布了新的文献求助10
15秒前
15秒前
16秒前
真实的雁风完成签到,获得积分10
16秒前
16秒前
16秒前
蔡宇滔发布了新的文献求助10
17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
Reducing Compassion Fatigue, Secondary Traumatic Stress and Burnout 600
Comparative Elite Sport Development Systems, Structures and Public Policy 600
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Auslegungsgeschichte 500
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7638018
求助须知:如何正确求助?哪些是违规求助? 9211365
关于积分的说明 19758586
捐赠科研通 7204977
什么是DOI,文献DOI怎么找? 3275778
关于科研通互助平台的介绍 2437385
邀请新用户注册赠送积分活动 2272936