Ryosuke Nagasawa, Kazumitsu Onizuka, Ryohei Iwata, Kosuke Tsuzuki, Kaoru R. Komatsu, Emi Miyashita, Sayaka Dantsuji, Hirotaka Murase, Hirohide Saito, Fumi Nagatsugi
RNA has emerged as an attractive target for drug discovery, increasing the importance of methods for identifying RNA-binding small molecules. Fluorescent indicator displacement (FID) assays are commonly used for screening such molecules. However, because fluorescent indicators detect hit compounds through competitive binding, developing a diverse range of indicators is essential to avoid missing potential hits. Here, we introduce novel RNA-binding fluorogenic molecular probes for FID assays by conjugating thiazole orange (TO) derivatives to the unique RNA-binding molecule G-clamp, resulting in TO-G-clamp. G-clamp was chosen for its distinct RNA-binding mode compared to TO derivatives, as demonstrated by their large-scale RNA-binding profiles. Four TO-G-clamp analogs were synthesized and evaluated, all retaining the broad RNA-binding selectivity of G-clamp. Among them, TO-G-clamp-Bn, which features a benzyl substituent on the TO moiety, exhibited the highest consistency with the RNA-binding selectivity of G-clamp. FID assays using TO-G-clamp-Bn identified unique hit compounds that were insensitive to the well-known indicator TO-PRO-1. Furthermore, SHAPE-MaP analysis revealed the RNA-binding sites of TO-G-clamp, TO-PRO-1, and one of the hit compounds, AZ191, showing that the binding sites of TO-G-clamp were in close proximity to those of AZ191.