Implement the Materials Genome Initiative: Machine Learning Assisted Fluorescent Probe Design for Cellular Substructure Staining

被引:1
|
作者
Yang, Yike [1 ,2 ]
Ji, Yumei [1 ]
Han, Xu [1 ]
Long, Yunxin [2 ]
Stewart, Callum [2 ]
Wen, Yiqiang [1 ]
Lee, Hok Yeung [2 ]
Cao, Tian [3 ]
Han, Jinsong [4 ]
Chen, Sijie [2 ]
Li, Linxian [2 ]
机构
[1] Zhengzhou Univ, Coll Chem & Green Catalysis Ctr, Zhengzhou 450000, Peoples R China
[2] Karolinska Inst, Ming Wai Lau Ctr Reparat Med, S-17177 Stockholm, Sweden
[3] Univ North Carolina Chapel Hill, Dept Comp Sci, Chapel Hill, NC 27599 USA
[4] China Pharmaceut Univ, Sch Engn, Nanjing 210009, Peoples R China
关键词
combinatorial library; fluorescent dyes; live-cell imaging; materials genomes; machine learning; ER; PERFORMANCE; DISCOVERY;
D O I
10.1002/admt.202300427
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The Materials Genome Initiative (MGI) is accelerating the pace of advanced materials development by integrating high-throughput experimentation, database construction, and intelligence computation. Live-cell imaging agents, such as fluorescent dyes, are exemplary candidates for MGI applications for two reasons: i) they are essential in visualizing cellular structures and functional processes, and ii) the unclear relationship between the chemical structure of fluorescent dyes and their live-cell imaging properties severely restricts the current trial-and-error dye development. Herein, the MGI is followed to present an intelligent combinatorial methodology for predicting the staining cell ability of dyes utilizing machine learning (ML) driven by a structurally diverse combinatorial library. This study demonstrates how to high-throughput synthesize 1,536 dyes and evaluate their imaging properties to establish a feature dataset for ML. A set of high-precision ML-predictors is then successfully modeled for assisting live-cell staining and endoplasmic reticulum judgment. This approach is believed to bridge the gap between dye structure and corresponding staining behavior, and can accelerate the discovery of novel organelle-specific stains.
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页数:10
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