Thirman Hannah L, Grider-Hayes Madeline J, Geben Laura C, Ihrie Rebecca A, Brown Lauren E, Porco John A, Irish Jonathan M
Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Chemical & Physical Biology Program, Vanderbilt University, Nashville, TN, USA.
Commun Biol. 2025 Jul 31;8(1):1137. doi: 10.1038/s42003-025-08545-3.
A challenge in chemical biology is to study structure-activity relationships (SAR) in vivo in cells. Multiplexed activity profiling (MAP), developed for natural product discovery, is well-suited to address this challenge as it is high throughput, singlecell, and measures multiple hallmark cellular functions. Applying MAP while systematically varying molecular structure (SAR-MAP) could reveal previously unappreciated activity within chemical families and prioritize candidate molecules for further characterization. Here we use SAR-MAP to identify structural features responsible for specific bioactivities of the natural product family, rocaglates. MV411 leukemia cells and healthy human leukocytes are selected for proof-of-concept screening. Testing 600 representative molecules using MAP classifies roughly half of tested rocaglates (9 of 19) as bioactive. SAR-MAP elucidates a methoxy substituent on select rocaglate pyrimidinones as responsible for a desirable anti-leukemia activity. Thus, SAR-MAP can be immediately applied to identify structural variations driving natural product activity in cell lines and primary human cells.
化学生物学面临的一个挑战是在细胞内研究结构-活性关系(SAR)。为天然产物发现而开发的多重活性分析(MAP)非常适合应对这一挑战,因为它具有高通量、单细胞特性,并且能够测量多种标志性细胞功能。在系统改变分子结构的同时应用MAP(SAR-MAP),可以揭示化学家族中以前未被认识到的活性,并为进一步表征确定候选分子的优先级。在这里,我们使用SAR-MAP来确定负责天然产物家族rocaglates特定生物活性的结构特征。选择MV411白血病细胞和健康人白细胞进行概念验证筛选。使用MAP测试600个代表性分子,大约一半的受试rocaglates(19个中的9个)被归类为具有生物活性。SAR-MAP阐明了选定的rocaglate嘧啶酮上的甲氧基取代基是产生理想抗白血病活性的原因。因此,SAR-MAP可立即用于识别驱动细胞系和原代人细胞中天然产物活性的结构变异。