pLM4CPPs: Protein Language Model-Based Predictor for Cell Penetrating Peptides

计算机科学 计算生物学 化学 人工智能 自然语言处理 生物
作者
Nandan Kumar,Zhenjiao Du,Yonghui Li
出处
期刊:Journal of Chemical Information and Modeling [American Chemical Society]
卷期号:65 (3): 1128-1139 被引量:10
标识
DOI:10.1021/acs.jcim.4c01338
摘要

Cell-penetrating peptides (CPPs) are short peptides capable of penetrating cell membranes, making them valuable for drug delivery and intracellular targeting. Accurate prediction of CPPs can streamline experimental validation in the lab. This study aims to assess pretrained protein language models (pLMs) for their effectiveness in representing CPPs and develop a reliable model for CPP classification. We evaluated peptide embeddings generated from BEPLER, CPCProt, SeqVec, various ESM variants (ESM, ESM-2 with expanded feature set, ESM-1b, and ESM-1v), ProtT5-XL UniRef50, ProtT5-XL BFD, and ProtBERT. We developed pLM4CCPs, a novel deep learning architecture using convolutional neural networks (CNNs) as the classifier for binary classification of CPPs. pLM4CCPs demonstrated superior performance over existing state-of-the-art CPP prediction models, achieving improvements in accuracy (ACC) by 4.9-5.5%, Matthews correlation coefficient (MCC) by 9.3-10.2%, and sensitivity (Sn) by 14.1-19.6%. Among all the tested models, ESM-1280 and ProtT5-XL BFD demonstrated the highest overall performance on the kelm data set. ESM-1280 achieved an ACC of 0.896, an MCC of 0.796, a Sn of 0.844, and a specificity (Sp) of 0.978. ProtT5-XL BFD exhibited superior performance with an ACC of 0.901, an MCC of 0.802, an Sn of 0.885, and an Sp of 0.917. pLM4CCPs combine predictions from multiple models to provide a consensus on whether a given peptide sequence is classified as a CPP or non-CPP. This approach will enhance prediction reliability by leveraging the strengths of each individual model. A user-friendly web server for bioactivity predictions, along with data sets, is available at https://ry2acnp6ep.us-east-1.awsapprunner.com. The source code and protocol for adapting pLM4CPPs can be accessed on GitHub at https://github.com/drkumarnandan/pLM4CPPs. This platform aims to advance CPP prediction and peptide functionality modeling, aiding researchers in exploring peptide functionality effectively.
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
爱生活完成签到,获得积分10
刚刚
团团团子完成签到 ,获得积分10
1秒前
2秒前
喜东东完成签到,获得积分10
2秒前
风中的樱桃完成签到,获得积分10
2秒前
3秒前
ding应助害羞的山晴采纳,获得30
4秒前
4秒前
科目三应助风中的樱桃采纳,获得10
5秒前
yiyi发布了新的文献求助10
5秒前
桐桐应助鳗鱼采纳,获得10
5秒前
盐汽水完成签到 ,获得积分10
6秒前
7秒前
zyy完成签到,获得积分10
7秒前
jerry发布了新的文献求助10
7秒前
7秒前
追风发布了新的文献求助10
8秒前
8秒前
surivoyage完成签到,获得积分10
8秒前
9秒前
Li发布了新的文献求助10
9秒前
9秒前
Arvin发布了新的文献求助10
9秒前
doppelganger发布了新的文献求助10
10秒前
kkkking发布了新的文献求助10
11秒前
11秒前
13秒前
LYQ完成签到,获得积分10
13秒前
赵梦然发布了新的文献求助10
14秒前
星辰大海应助Lina采纳,获得10
14秒前
核桃发布了新的文献求助10
14秒前
15秒前
doppelganger发布了新的文献求助10
16秒前
16秒前
鳗鱼发布了新的文献求助10
17秒前
我是老大应助松饼采纳,获得10
18秒前
Archie应助kd采纳,获得10
19秒前
relaxact完成签到 ,获得积分10
19秒前
小二郎应助kkkking采纳,获得10
20秒前
20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
Modern Epidemiology, Fourth Edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
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 6025081
求助须知:如何正确求助?哪些是违规求助? 7659914
关于积分的说明 16178336
捐赠科研通 5173305
什么是DOI,文献DOI怎么找? 2768128
邀请新用户注册赠送积分活动 1751546
关于科研通互助平台的介绍 1637642