表位
计算机科学
分类器(UML)
计算生物学
人工智能
线性表位
生成语法
表位定位
蛋白质测序
机器学习
序列(生物学)
生成模型
发电机(电路理论)
模式识别(心理学)
统计模型
模拟电影
统计假设检验
抗原
翻译(生物学)
肽序列
线性判别分析
班级(哲学)
免疫识别
作者
Natalia Flechas Manrique,Alberto Martínez,Elena López‐Martínez,Luc Andrea,Román Orús,Aitor Manteca,Aitziber L. Cortajarena,Llorenç Espinosa-Portalés
标识
DOI:10.1021/acssynbio.5c00693
摘要
amino acids, making screening and testing unfeasible, even with high throughput experimental techniques. In this study, we present a large language model, epiGPTope, pretrained on protein data and specifically fine-tuned on linear epitopes, which, for the first time, can directly generate novel epitope-like sequences, which are found to possess statistical properties analogous to the ones of known epitopes. This generative approach can be used to prepare libraries of epitope candidate sequences. We further train statistical classifiers to predict whether an epitope sequence is of bacterial or viral origin, thus narrowing the candidate library and increasing the likelihood of identifying specific epitopes. We propose that such a combination of generative and predictive models can be of assistance in epitope discovery. The approach uses only primary amino acid sequences of linear epitopes, bypassing the need for a geometric framework or handcrafted features of the sequences. By developing a method to create biologically feasible sequences, we anticipate faster and more cost-effective generation and screening of synthetic epitopes with relevant applications in the development of new biotechnologies.
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