High-throughput functional annotation of natural products by integrated activity profiling

计算生物学 代谢组学 天然产物 药物发现 仿形(计算机编程) 生物 系统生物学 注释 计算机科学 生物信息学 生物化学 操作系统
作者
Suzie K. Hight,Trevor N. Clark,Kenji L. Kurita,Elizabeth A. McMillan,Walter M. Bray,Anam F. Shaikh,Aswad S Khadilkar,F. P. Jake Haeckl,Fausto Carnevale Neto,Scott La,Akshar Lohith,Rachel M. Vaden,Jeon Lee,Shuguang Wei,R. Scott Lokey,Michael A. White,Roger G. Linington,John B. MacMillan
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:119 (49) 被引量:3
标识
DOI:10.1073/pnas.2208458119
摘要

Determining mechanism of action (MOA) is one of the biggest challenges in natural products discovery. Here, we report a comprehensive platform that uses Similarity Network Fusion (SNF) to improve MOA predictions by integrating data from the cytological profiling high-content imaging platform and the gene expression platform Functional Signature Ontology, and pairs these data with untargeted metabolomics analysis for de novo bioactive compound discovery. The predictive value of the integrative approach was assessed using a library of target-annotated small molecules as benchmarks. Using Kolmogorov-Smirnov (KS) tests to compare in-class to out-of-class similarity, we found that SNF retains the ability to identify significant in-class similarity across a diverse set of target classes, and could find target classes not detectable in either platform alone. This confirmed that integration of expression-based and image-based phenotypes can accurately report on MOA. Furthermore, we integrated untargeted metabolomics of complex natural product fractions with the SNF network to map biological signatures to specific metabolites. Three examples are presented where SNF coupled with metabolomics was used to directly functionally characterize natural products and accelerate identification of bioactive metabolites, including the discovery of the azoxy-containing biaryl compounds parkamycins A and B. Our results support SNF integration of multiple phenotypic screening approaches along with untargeted metabolomics as a powerful approach for advancing natural products drug discovery.

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