Department of Automation, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Minhang District, Shanghai 200240, China.
Department of Rheumatology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, No. 1630 East Road, Pudong New Area, Shanghai 200127, China.
Brief Bioinform. 2024 Sep 23;25(6). doi: 10.1093/bib/bbae525.
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.
设计具有特定生物活性的全新分子是一项至关重要的任务,因为它有可能绕过现代药物发现范例中探索目标基因这一初始步骤。然而,传统方法主要通过比较文献中记载的实验结果内期望的分子效应来筛选分子。数据集限制了这个过程,而且很难进行直接的跨模态比较。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),它仅使用基因表达特征生成类似命中的分子。这些特征是通过输入对照和期望的基因表达状态来计算的。我们的模型 GexMolGen 采用“先对齐再生成”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,以确保生成的所有分子都是 100%有效的。实证结果表明,无论输入的是同源或异源转录组数据,我们的模型都可以生成与已知参考文献高度相似的分子。此外,它还可以作为一种可靠的跨模态筛选工具。