A multi-agent system for automating scientific discovery | Nature
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A multi-agent system for automating scientific discovery
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Computational platforms and environments<br>Target identification
Abstract<br>Scientific discovery is driven by the iterative process of observation, hypothesis generation, experimentation, and data analysis. Despite recent advancements in applying artificial intelligence to biology, no system has yet automated all these stages [1, 2, 3]. Here, we introduce Robin, the first multi-agent system capable of fully automating both hypothesis generation and data analysis for experimental biology. By integrating literature search agents with data analysis agents, Robin can generate hypotheses, propose experiments, interpret experimental results, and generate updated hypotheses, achieving a semi-autonomous approach to scientific discovery. By applying this system, we were able to identify promising therapeutic candidates for dry age-related macular degeneration (dAMD), the major cause of blindness in the developed world [4, 5]. Robin proposed enhancing retinal pigment epithelium phagocytosis as a therapeutic strategy, and identified and confirmed in vitro efficacy for ripasudil and KL001. Ripasudil is a clinically-used Rho kinase (ROCK) inhibitor that has never previously been proposed for treating dAMD. To elucidate the mechanism of ripasudil-induced upregulation of phagocytosis, Robin then proposed and analyzed a follow-up RNA-seq experiment, which revealed upregulation of ABCA1, a lipid efflux pump and possible novel target. All hypotheses, experimental directions, data analyses, and data figures in the main text of this report were produced by Robin. As the first AI system to autonomously discover and validate novel therapeutic candidates within an iterative lab-in-the-loop framework, Robin establishes a new paradigm for AI-driven scientific discovery.
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Author information<br>Author notesThese authors contributed equally: Ali Essam Ghareeb, Benjamin Chang
These authors jointly supervised this work: Andrew D. White, Michaela M. Hinks, Samuel G. Rodriques
Authors and Affiliations<br>FutureHouse, San Francisco, USA<br>Ali Essam Ghareeb, Benjamin Chang, Ludovico Mitchener, Angela Yiu, Caralyn J. Szostkiewicz, Jon M. Laurent, Samantha M. Wright, Muhammed T. Razzak, Andrew D. White, Silvia C. Finnemann, Michaela M. Hinks & Samuel G. Rodriques
University of Oxford, Oxford, UK<br>Benjamin Chang
Fordham University, New York, USA<br>Dmytro Shved & Gavin J. Gyimesi
AuthorsAli Essam GhareebView author publications<br>Search author on:PubMed Google Scholar
Benjamin ChangView author publications<br>Search author on:PubMed Google Scholar
Ludovico MitchenerView author publications<br>Search author on:PubMed Google Scholar
Angela YiuView author publications<br>Search author on:PubMed Google Scholar
Caralyn J. SzostkiewiczView author publications<br>Search author on:PubMed Google Scholar
Dmytro ShvedView author publications<br>Search author on:PubMed Google Scholar
Gavin J. GyimesiView author publications<br>Search author on:PubMed Google Scholar
Jon M. LaurentView author publications<br>Search author on:PubMed Google Scholar
Samantha M. WrightView author publications<br>Search author on:PubMed Google Scholar
Muhammed T. RazzakView author publications<br>Search author on:PubMed Google Scholar
Andrew D. WhiteView author publications<br>Search author on:PubMed Google Scholar
Silvia C. FinnemannView author publications<br>Search author on:PubMed Google Scholar
Michaela M. HinksView author publications<br>Search author on:PubMed Google Scholar
Samuel G. RodriquesView author publications<br>Search author on:PubMed Google Scholar
Corresponding authors<br>Correspondence to<br>Andrew D. White, Michaela M. Hinks or Samuel G. Rodriques.
Supplementary information
Supplementary Information (download PDF )<br>Combined PDF containing Supplementary Tables 1-2, Supplementary Figures 1-20, and Supplementary References. The tables list drugs with working concentrations and antibodies used in this paper. The figures detail...