基于 BERT 和 LLM 的 avGFP 亮度预测和突变设计

X. Guo, W. Che
{"title":"基于 BERT 和 LLM 的 avGFP 亮度预测和突变设计","authors":"X. Guo, W. Che","doi":"arxiv-2407.20534","DOIUrl":null,"url":null,"abstract":"This study aims to utilize Transformer models and large language models (such\nas GPT and Claude) to predict the brightness of Aequorea victoria green\nfluorescent protein (avGFP) and design mutants with higher brightness.\nConsidering the time and cost associated with traditional experimental\nscreening methods, this study employs machine learning techniques to enhance\nresearch efficiency. We first read and preprocess a proprietary dataset\ncontaining approximately 140,000 protein sequences, including about 30,000\navGFP sequences. Subsequently, we constructed and trained a Transformer-based\nprediction model to screen and design new avGFP mutants that are expected to\nexhibit higher brightness. Our methodology consists of two primary stages: first, the construction of a\nscoring model using BERT, and second, the screening and generation of mutants\nusing mutation site statistics and large language models. Through the analysis\nof predictive results, we designed and screened 10 new high-brightness avGFP\nsequences. This study not only demonstrates the potential of deep learning in\nprotein design but also provides new perspectives and methodologies for future\nresearch by integrating prior knowledge from large language models.","PeriodicalId":501219,"journal":{"name":"arXiv - QuanBio - Other Quantitative Biology","volume":"20 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"BERT and LLMs-Based avGFP Brightness Prediction and Mutation Design\",\"authors\":\"X. Guo, W. Che\",\"doi\":\"arxiv-2407.20534\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study aims to utilize Transformer models and large language models (such\\nas GPT and Claude) to predict the brightness of Aequorea victoria green\\nfluorescent protein (avGFP) and design mutants with higher brightness.\\nConsidering the time and cost associated with traditional experimental\\nscreening methods, this study employs machine learning techniques to enhance\\nresearch efficiency. We first read and preprocess a proprietary dataset\\ncontaining approximately 140,000 protein sequences, including about 30,000\\navGFP sequences. Subsequently, we constructed and trained a Transformer-based\\nprediction model to screen and design new avGFP mutants that are expected to\\nexhibit higher brightness. Our methodology consists of two primary stages: first, the construction of a\\nscoring model using BERT, and second, the screening and generation of mutants\\nusing mutation site statistics and large language models. Through the analysis\\nof predictive results, we designed and screened 10 new high-brightness avGFP\\nsequences. This study not only demonstrates the potential of deep learning in\\nprotein design but also provides new perspectives and methodologies for future\\nresearch by integrating prior knowledge from large language models.\",\"PeriodicalId\":501219,\"journal\":{\"name\":\"arXiv - QuanBio - Other Quantitative Biology\",\"volume\":\"20 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Other Quantitative Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2407.20534\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Other Quantitative Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2407.20534","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

考虑到传统实验筛选方法的时间和成本,本研究采用机器学习技术来提高研究效率。我们首先读取并预处理了一个专有数据集,该数据集包含约 140,000 个蛋白质序列,其中包括约 30,000 个avGFP 序列。随后,我们构建并训练了一个基于 Transformer 的预测模型,用于筛选和设计有望表现出更高亮度的新 avGFP 突变体。我们的方法包括两个主要阶段:首先,利用 BERT 构建 ascoring 模型;其次,利用突变位点统计和大型语言模型筛选和生成突变体。通过分析预测结果,我们设计并筛选出了 10 个新的高亮度 avGFP 序列。这项研究不仅展示了深度学习在蛋白质设计方面的潜力,而且通过整合大型语言模型的先验知识,为未来研究提供了新的视角和方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BERT and LLMs-Based avGFP Brightness Prediction and Mutation Design
This study aims to utilize Transformer models and large language models (such as GPT and Claude) to predict the brightness of Aequorea victoria green fluorescent protein (avGFP) and design mutants with higher brightness. Considering the time and cost associated with traditional experimental screening methods, this study employs machine learning techniques to enhance research efficiency. We first read and preprocess a proprietary dataset containing approximately 140,000 protein sequences, including about 30,000 avGFP sequences. Subsequently, we constructed and trained a Transformer-based prediction model to screen and design new avGFP mutants that are expected to exhibit higher brightness. Our methodology consists of two primary stages: first, the construction of a scoring model using BERT, and second, the screening and generation of mutants using mutation site statistics and large language models. Through the analysis of predictive results, we designed and screened 10 new high-brightness avGFP sequences. This study not only demonstrates the potential of deep learning in protein design but also provides new perspectives and methodologies for future research by integrating prior knowledge from large language models.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信