{"title":"Mapping the combinatorial coding between olfactory receptors and perception with deep learning","authors":"Seyone Chithrananda, Judith Amores, Kevin K Yang","doi":"10.1101/2024.09.16.613334","DOIUrl":null,"url":null,"abstract":"The sense of smell remains poorly understood, especially in contrast to visual and auditory coding. At the core of our sense of smell is the olfactory information flow, in which odorant molecules activate a subset of our olfactory receptors and combinations of unique receptor activations code for unique odors. Understanding this relationship is crucial for unraveling the mysteries of human olfaction and its potential therapeutic applications. Despite this, predicting molecule-OR interactions remains incredibly difficult. Here, we develop a novel, biologically-inspired approach that first maps odorant molecules to their respective OR activation profiles and subsequently predicts their odor percepts. Despite a lack of overlap between molecules with OR activation data and percept annotations, our joint model improves percept prediction by leveraging the OR activation profile of each odorant as auxiliary features in predicting its percepts. We extend this cross receptor-percept approach, showing that sets of molecules with very different structures but similar percepts, a common challenge for chemosensory prediction, have similar predicted OR activation profiles. Lastly, we further probe the odorant-OR model's predictive ability, showing it can distinguish binding patterns across unique OR families, as well as between protein-coding genes or frequently occuring pseudogenes in the human olfactory subgenome. This work may aid in the potential discovery of novel odorant ligands targeting functions of orphan ORs, and in further characterizing the relationship between chemical structures and percepts. In doing so, we hope to advance our understanding of olfactory perception and the design of new odorants with desired perceptual qualities.","PeriodicalId":501108,"journal":{"name":"bioRxiv - Molecular Biology","volume":"16 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.16.613334","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The sense of smell remains poorly understood, especially in contrast to visual and auditory coding. At the core of our sense of smell is the olfactory information flow, in which odorant molecules activate a subset of our olfactory receptors and combinations of unique receptor activations code for unique odors. Understanding this relationship is crucial for unraveling the mysteries of human olfaction and its potential therapeutic applications. Despite this, predicting molecule-OR interactions remains incredibly difficult. Here, we develop a novel, biologically-inspired approach that first maps odorant molecules to their respective OR activation profiles and subsequently predicts their odor percepts. Despite a lack of overlap between molecules with OR activation data and percept annotations, our joint model improves percept prediction by leveraging the OR activation profile of each odorant as auxiliary features in predicting its percepts. We extend this cross receptor-percept approach, showing that sets of molecules with very different structures but similar percepts, a common challenge for chemosensory prediction, have similar predicted OR activation profiles. Lastly, we further probe the odorant-OR model's predictive ability, showing it can distinguish binding patterns across unique OR families, as well as between protein-coding genes or frequently occuring pseudogenes in the human olfactory subgenome. This work may aid in the potential discovery of novel odorant ligands targeting functions of orphan ORs, and in further characterizing the relationship between chemical structures and percepts. In doing so, we hope to advance our understanding of olfactory perception and the design of new odorants with desired perceptual qualities.
人们对嗅觉的了解仍然很少,尤其是与视觉和听觉编码相比。嗅觉的核心是嗅觉信息流,其中气味分子激活嗅觉受体的一个子集,独特的受体激活组合编码出独特的气味。了解这种关系对于揭开人类嗅觉及其潜在治疗应用的神秘面纱至关重要。尽管如此,预测分子与嗅觉受体之间的相互作用仍然非常困难。在这里,我们开发了一种新颖的、受生物学启发的方法,首先将气味分子映射到它们各自的OR激活图谱,然后预测它们的气味感知。尽管分子与受体活化数据和知觉注释之间缺乏重叠,但我们的联合模型利用每种气味的受体活化特征作为预测其知觉的辅助特征,从而改进了知觉预测。我们扩展了这种跨受体-知觉的方法,表明结构迥异但知觉相似的分子集(这是化感预测面临的一个常见挑战)具有相似的预测 OR 激活曲线。最后,我们进一步探究了气味-OR 模型的预测能力,结果表明它可以区分独特的 OR 家族之间的结合模式,以及人类嗅觉亚基因组中的蛋白编码基因或频繁出现的假基因之间的结合模式。这项工作可能有助于发现针对孤儿 OR 功能的新型气味配体,并进一步确定化学结构与感知之间的关系。在此过程中,我们希望加深对嗅觉感知的理解,并设计出具有理想感知品质的新型气味剂。