GexMolGen: cross-modal generation of hit-like molecules via large language model encoding of gene expression signatures

Designing de novo molecules with specific biological activity is an essential task since it holds the potential to bypass the exploration of target genes, which is an initial step in the modern drug discovery paradigm. However, traditional methods mainly screen molecules by comparing the desired molecular effects within the documented experimental results. The data set limits this process, and it is hard to conduct direct cross-modal comparisons. Therefore, we propose a solution based on cross-modal generation called GexMolGen (Gene Expression-based Molecule Generator), which generates hit-like molecules using gene expression signatures alone. These signatures are calculated by inputting control and desired gene expression states. Our model GexMolGen adopts a "first-align-then-generate" strategy, aligning the gene expression signatures and molecules within a mapping space, ensuring a smooth cross-modal transition. The transformed molecular embeddings are then decoded into molecular graphs. In addition, we employ an advanced single-cell large language model for input flexibility and pre-train a scaffold-based molecular model to ensure that all generated molecules are 100% valid. Empirical results show that our model can produce molecules highly similar to known references, whether feeding in- or out-of-domain transcriptome data. Furthermore, it can also serve as a reliable tool for cross-modal screening.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/bib/bbae525
Citations
8
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
2.89

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article

GexMolGen: cross-modal generation of hit-like molecules via large language model encoding of gene expression signatures

Yiming Xue, Qingran Yan, Ye Yuan, Jiabei Cheng et al.
8 citations
Briefings in Bioinformatics
Computational Drug Discovery Methods
2.89
article

GexMolGen: cross-modal generation of hit-like molecules via large language model encoding of gene expression signatures

Yiming Xue, Qingran Yan, Ye Yuan, Jiabei Cheng, Xiaoyong Pan, Yi Fang, Kaiyuan Yang
article en
8 citations

Abstract

Designing de novo molecules with specific biological activity is an essential task since it holds the potential to bypass the exploration of target genes, which is an initial step in the modern drug discovery paradigm. However, traditional methods mainly screen molecules by comparing the desired molecular effects within the documented experimental results. The data set limits this process, and it is hard to conduct direct cross-modal comparisons. Therefore, we propose a solution based on cross-modal generation called GexMolGen (Gene Expression-based Molecule Generator), which generates hit-like molecules using gene expression signatures alone. These signatures are calculated by inputting control and desired gene expression states. Our model GexMolGen adopts a "first-align-then-generate" strategy, aligning the gene expression signatures and molecules within a mapping space, ensuring a smooth cross-modal transition. The transformed molecular embeddings are then decoded into molecular graphs. In addition, we employ an advanced single-cell large language model for input flexibility and pre-train a scaffold-based molecular model to ensure that all generated molecules are 100% valid. Empirical results show that our model can produce molecules highly similar to known references, whether feeding in- or out-of-domain transcriptome data. Furthermore, it can also serve as a reliable tool for cross-modal screening.

Briefings in BioinformaticsVol. 25(6)
Shanghai Jiao Tong University (CN), Chinese Academy of Sciences (CN), Renji Hospital (CN), Institute of Process Engineering (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 8%
Computational Drug Discovery Methods
2.89
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