Wang Ting, Cook Ian, Leyh Thomas S
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York 10461-1926.
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York 10461-1926.
J Biol Chem. 2017 Dec 8;292(49):20305-20312. doi: 10.1074/jbc.M117.817387. Epub 2017 Oct 16.
Non-steroidal anti-inflammatory drugs (NSAIDs) are among the most commonly prescribed drugs worldwide-more than 111 million prescriptions were written in the United States in 2014. NSAIDs allosterically inhibit cytosolic sulfotransferases (SULTs) with high specificity and therapeutically relevant affinities. This study focuses on the interactions of SULT1A1 and mefenamic acid (MEF)-a potent, highly specific NSAID inhibitor of 1A1. Here, the first structure of an NSAID allosteric site-the MEF-binding site of SULT1A1-is determined using spin-label triangulation NMR. The structure is confirmed by site-directed mutagenesis and provides a molecular framework for understanding NSAID binding and isoform specificity. The mechanism of NSAID inhibition is explored using molecular dynamics and equilibrium and pre-steady-state ligand-binding studies. MEF inhibits SULT1A1 turnover through an indirect (helix-mediated) stabilization of the closed form of the active-site cap of the enzyme, which traps the nucleotide and slows its release. Using the NSAID-binding site structure of SULT1A1 as a comparative model, it appears that 11 of the 13 human SULT isoforms harbor an NSAID-binding site. We hypothesize that these sites evolved to enable SULT isoforms to respond to metabolites that lie within their metabolic domains. Finally, the NSAID-binding site structure offers a template for developing isozyme-specific allosteric inhibitors that can be used to regulate specific areas of sulfuryl-transfer metabolism.
非甾体抗炎药(NSAIDs)是全球处方量最多的药物之一——2014年美国开出了超过1.11亿份处方。NSAIDs以高特异性和与治疗相关的亲和力变构抑制胞质磺基转移酶(SULTs)。本研究聚焦于SULT1A1与甲芬那酸(MEF)的相互作用——MEF是一种强效、高特异性的1A1 NSAID抑制剂。在此,利用自旋标记三角测量核磁共振确定了NSAID变构位点的首个结构——SULT1A1的MEF结合位点。该结构通过定点诱变得到证实,并为理解NSAID结合和同工型特异性提供了分子框架。利用分子动力学以及平衡和预稳态配体结合研究探索了NSAID抑制机制。MEF通过间接(螺旋介导)稳定酶活性位点帽的封闭形式来抑制SULT1A1的周转,这种封闭形式会捕获核苷酸并减缓其释放。以SULT1A1的NSAID结合位点结构作为比较模型,似乎13种人类SULT同工型中有11种具有NSAID结合位点。我们推测这些位点的进化是为了使SULT同工型能够对其代谢域内的代谢物做出反应。最后,NSAID结合位点结构为开发可用于调节磺基转移代谢特定区域的同工酶特异性变构抑制剂提供了模板。