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基于蛋白质内在无序区域的无监督深度学习生成促进成骨的功能性寡肽。

Generation of functional oligopeptides that promote osteogenesis based on unsupervised deep learning of protein IDRs.

作者信息

Cai Mingxiang, Xiao Baichuan, Jin Fujun, Xu Xiaopeng, Hua Yuwei, Li Junhui, Niu Pingping, Liu Meijing, Wu Jiaqi, Yue Rui, Zhang Yong, Wang Zuolin, Zhang Yongbiao, Wang Xiaogang, Sun Yao

机构信息

Department of Oral Implantology, School of Stomatology, Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, 200072, China.

The First Affiliated Hospital of Jinan University, School of Stomatology, Clinical Research Platform for Interdiscipline of Stomatology, Jinan University, Guangzhou, 510630, China.

出版信息

Bone Res. 2022 Mar 1;10(1):23. doi: 10.1038/s41413-022-00193-1.

DOI:10.1038/s41413-022-00193-1
PMID:35228528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8885677/
Abstract

Deep learning (DL) is currently revolutionizing peptide drug development due to both computational advances and the substantial recent expansion of digitized biological data. However, progress in oligopeptide drug development has been limited, likely due to the lack of suitable datasets and difficulty in identifying informative features to use as inputs for DL models. Here, we utilized an unsupervised deep learning model to learn a semantic pattern based on the intrinsically disordered regions of ~171 known osteogenic proteins. Subsequently, oligopeptides were generated from this semantic pattern based on Monte Carlo simulation, followed by in vivo functional characterization. A five amino acid oligopeptide (AIB5P) had strong bone-formation-promoting effects, as determined in multiple mouse models (e.g., osteoporosis, fracture, and osseointegration of implants). Mechanistically, we showed that AIB5P promotes osteogenesis by binding to the integrin α5 subunit and thereby activating FAK signaling. In summary, we successfully established an oligopeptide discovery strategy based on a DL model and demonstrated its utility from cytological screening to animal experimental verification.

摘要

由于计算技术的进步以及近期数字化生物数据的大量扩充,深度学习(DL)目前正在彻底改变肽类药物的开发。然而,寡肽药物开发的进展有限,这可能是由于缺乏合适的数据集以及难以识别用作DL模型输入的信息性特征。在此,我们利用无监督深度学习模型基于约171种已知成骨蛋白的内在无序区域学习语义模式。随后,基于蒙特卡罗模拟从该语义模式生成寡肽,接着进行体内功能表征。在多个小鼠模型(如骨质疏松症、骨折和植入物骨整合)中确定,一种五氨基酸寡肽(AIB5P)具有强大的促进骨形成作用。从机制上讲,我们表明AIB5P通过与整合素α5亚基结合从而激活FAK信号来促进成骨。总之,我们成功建立了一种基于DL模型的寡肽发现策略,并证明了其从细胞学筛选到动物实验验证的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/616eb0814f37/41413_2022_193_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/06654e3d36a9/41413_2022_193_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/baec4d1e8b35/41413_2022_193_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/1bf50bf9937d/41413_2022_193_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/31d5d49a4270/41413_2022_193_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/a45b04d211d1/41413_2022_193_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/616eb0814f37/41413_2022_193_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/06654e3d36a9/41413_2022_193_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/baec4d1e8b35/41413_2022_193_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/1bf50bf9937d/41413_2022_193_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/31d5d49a4270/41413_2022_193_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/a45b04d211d1/41413_2022_193_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3011/8885677/616eb0814f37/41413_2022_193_Fig6_HTML.jpg

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