Department of Pharmacy, Center for Drug Research, Ludwig-Maximilians-Universität Munich, Butenandtstraße 7, 81377, Munich, Germany.
ChemMedChem. 2021 Jan 8;16(1):199-215. doi: 10.1002/cmdc.202000342. Epub 2020 Sep 10.
This study describes the first binding assay for glycine transporter 2 (GlyT2) following the concept of MS Binding Assays. The selective GlyT2 inhibitor Org25543 was employed as a reporter ligand and it was quantified with a highly sensitive and rapid LC-ESI-MS/MS method. Binding of Org25543 at GlyT2 was characterized in kinetic and saturation experiments with an off-rate of 7.07×10 s , an on-rate of 1.01×10 M s , and an equilibrium dissociation constant of 7.45 nM. Furthermore, the inhibitory constants of 19 GlyT ligands were determined in competition experiments. The validity of the GlyT2 affinities determined with the binding assay was examined by a comparison with published inhibitory potencies from various functional assays. With the capability for affinity determination towards GlyT2 the developed MS Binding Assays provide the first tool for affinity profiling of potential ligands and it represents a valuable new alternative to functional assays addressing GlyT2.
本研究描述了基于 MS 结合测定概念的甘氨酸转运体 2(GlyT2)的首次结合测定。选择甘氨酸转运体 2 抑制剂 Org25543 作为报告配体,并采用高灵敏度和快速的 LC-ESI-MS/MS 方法进行定量。通过动力学和饱和实验,对 Org25543 在 GlyT2 上的结合进行了特征描述,其离解速率常数为 7.07×10 s ,进入速率常数为 1.01×10 M s ,平衡解离常数为 7.45 nM。此外,还在竞争实验中测定了 19 种甘氨酸转运体配体的抑制常数。通过与各种功能测定中发表的抑制效力进行比较,检验了结合测定中确定的 GlyT2 亲和力的有效性。该结合测定具有对 GlyT2 亲和力进行测定的能力,为潜在配体的亲和力分析提供了首个工具,代表了一种有价值的新替代方法,可替代针对 GlyT2 的功能测定。