Shipton Megan L, Jamion Fathima A, Wheeler Simon, Riley Andrew M, Plasser Felix, Potter Barry V L, Butler Stephen J
Medicinal Chemistry & Drug Discovery, Department of Pharmacology, University of Oxford Mansfield Road Oxford OX1 3QT UK
Department of Chemistry, Loughborough University Epinal Way, Loughborough LE11 3TU UK
Chem Sci. 2023 Apr 13;14(19):4979-4985. doi: 10.1039/d2sc06812e. eCollection 2023 May 17.
Inositol pyrophosphates are important biomolecules associated with apoptosis, cell growth and kinase regulation, yet their exact biological roles are still emerging and probes do not exist for their selective detection. We report the first molecular probe for the selective and sensitive detection of the most abundant cellular inositol pyrophosphate 5-PP-InsP, as well as an efficient new synthesis. The probe is based on a macrocyclic Eu(iii) complex bearing two quinoline arms providing a free coordination site at the Eu(iii) metal centre. Bidentate binding of the pyrophosphate group of 5-PP-InsP to the Eu(iii) ion is proposed, supported by DFT calculations, giving rise to a selective enhancement in Eu(iii) emission intensity and lifetime. We demonstrate the use of time-resolved luminescence as a bioassay tool for monitoring enzymatic processes in which 5-PP-InsP is consumed. Our probe offers a potential screening methodology to identify drug-like compounds that modulate the activity of enzymes of inositol pyrophosphate metabolism.
肌醇焦磷酸是与细胞凋亡、细胞生长和激酶调节相关的重要生物分子,但其确切的生物学作用仍在不断显现,且不存在用于其选择性检测的探针。我们报道了首个用于选择性、灵敏检测细胞中最丰富的肌醇焦磷酸5-PP-InsP的分子探针,以及一种高效的新合成方法。该探针基于一种带有两个喹啉臂的大环铕(III)配合物,在铕(III)金属中心提供一个自由配位位点。密度泛函理论计算支持5-PP-InsP的焦磷酸基团与铕(III)离子的双齿结合,导致铕(III)发射强度和寿命的选择性增强。我们展示了将时间分辨发光用作生物测定工具,以监测5-PP-InsP被消耗的酶促过程。我们的探针提供了一种潜在的筛选方法,用于鉴定调节肌醇焦磷酸代谢酶活性的类药物化合物。