GexMolGen:通过对基因表达特征的大型语言模型编码,跨模态生成命中类分子。

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Jiabei Cheng, Xiaoyong Pan, Yi Fang, Kaiyuan Yang, Yiming Xue, Qingran Yan, Ye Yuan
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引用次数: 0

摘要

设计具有特定生物活性的全新分子是一项重要任务,因为它有可能绕过靶基因的探索,这是现代药物发现范式的第一步。然而,传统方法主要通过比较实验结果记录中的预期分子效应来筛选分子。数据集限制了这一过程,而且很难进行直接的跨模式比较。因此,我们提出了一种基于跨模态生成的解决方案,称为 GexMolGen(基于基因表达的分子生成器),它仅通过基因表达特征就能生成热门分子。这些特征是通过输入控制和期望的基因表达状态计算出来的。我们的 GexMolGen 模型采用 "先对齐后生成 "的策略,在映射空间内对齐基因表达特征和分子,确保平滑的跨模态转换。然后将转换后的分子嵌入解码为分子图。此外,我们还采用了先进的单细胞大语言模型来提高输入的灵活性,并预先训练基于支架的分子模型,以确保所有生成的分子都是 100% 有效的。实证结果表明,我们的模型可以生成与已知参考文献高度相似的分子,无论是输入域内还是域外转录组数据。此外,它还可以作为跨模态筛选的可靠工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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