Abteilung für Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Straße 11, 44227, Dortmund, Germany.
Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Straße 6, 44227, Dortmund, Germany.
Angew Chem Int Ed Engl. 2017 Oct 9;56(42):13021-13025. doi: 10.1002/anie.201707394. Epub 2017 Sep 18.
Cell-based assays enable monitoring of small-molecule bioactivity in a target-agnostic manner and help uncover new biological mechanisms. Subsequent identification and validation of the small-molecule targets, typically employing proteomics techniques, is very challenging and limited, in particular if the targets are membrane proteins. Herein, we demonstrate that the combination of cell-based bioactive-compound discovery with cheminformatic target prediction may provide an efficient approach to accelerate the process and render target identification and validation more efficient. Using a cell-based assay, we identified the pyrazolo-imidazole smoothib as a new inhibitor of hedgehog (Hh) signaling and an antagonist of the protein smoothened (SMO) with a novel chemotype. Smoothib targets the heptahelical bundle of SMO, prevents its ciliary localization, reduces the expression of Hh target genes, and suppresses the growth of Ptch medulloblastoma cells.
基于细胞的测定法可实现以无靶标方式监测小分子的生物活性,有助于揭示新的生物学机制。随后,通常采用蛋白质组学技术对小分子靶标进行鉴定和验证,但这非常具有挑战性且受限,特别是如果靶标是膜蛋白。在此,我们证明了基于细胞的生物活性化合物发现与计算化学靶标预测的结合,可能是一种加速这一过程并使靶标鉴定和验证更有效的有效方法。我们使用基于细胞的测定法,鉴定出吡唑并咪唑类 smoothenin 拮抗剂 smoothib 是 hedgehog (Hh) 信号的新型抑制剂,其具有新型化学型。Smoothib 靶向 SMO 的七螺旋束,阻止其在纤毛中的定位,降低 Hh 靶基因的表达,并抑制 Ptch 髓母细胞瘤细胞的生长。