Division of Biophysics, Institute of Experimental Physics, Faculty of Physics, University of Warsaw, Pasteura 5, 02-093 Warsaw, Poland.
Centre of New Technologies University of Warsaw, Banacha 2c, 02-097 Warsaw, Poland.
ACS Chem Biol. 2022 Mar 18;17(3):661-669. doi: 10.1021/acschembio.1c00978. Epub 2022 Feb 23.
Sulfotransferases (STs) are ubiquitous enzymes that participate in a vast number of biological processes involving sulfuryl group (SO) transfer. 3'-phosphoadenosine 5'-phosphosulfate (PAPS) is the universal ST cofactor, serving as the "active sulfate" source in cells. Herein, we report the synthesis of three fluorinated PAPS analogues that bear fluorine or trifluoromethyl substituents at the C2 or C8 positions of adenine and their evaluation as substitute cofactors that enable ST activity to be quantified and real-time-monitored by fluorine-19 nuclear magnetic resonance (F NMR) spectroscopy. Using plant AtSOT18 and human SULT1A3 as two model enzymes, we reveal that the fluorinated PAPS analogues show complementary properties with regard to recognition by enzymes and the working F NMR pH range and are attractive versatile tools for studying STs. Finally, we developed an F NMR assay for screening potential inhibitors against SULT1A3, thereby highlighting the possible use of fluorinated PAPS analogues for the discovery of drugs for ST-related diseases.
磺基转移酶(STs)是广泛存在的酶,参与涉及硫基(SO)转移的大量生物过程。3'-磷酸腺苷 5'-磷酸硫酸(PAPS)是通用的 ST 辅酶,是细胞中“活性硫酸盐”的来源。在此,我们报告了三种氟化 PAPS 类似物的合成,这些类似物在腺嘌呤的 C2 或 C8 位置带有氟或三氟甲基取代基,并评估了它们作为替代辅酶的作用,通过氟-19 核磁共振(F NMR)光谱可定量和实时监测 ST 活性。使用植物 AtSOT18 和人 SULT1A3 作为两种模型酶,我们揭示了氟化 PAPS 类似物在与酶的识别以及工作 F NMR pH 范围方面具有互补特性,是研究 STs 的有吸引力的通用工具。最后,我们开发了一种用于筛选针对 SULT1A3 的潜在抑制剂的 F NMR 测定法,从而突出了氟化 PAPS 类似物在发现与 ST 相关疾病的药物方面的可能用途。