Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California.
Howard Hughes Medical Institute and Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California.
Protein Sci. 2019 Oct;28(10):1750-1757. doi: 10.1002/pro.3694. Epub 2019 Aug 9.
The bacterial periplasmic methionine-binding protein MetQ is involved in the import of methionine by the cognate MetNI methionine ATP binding cassette (ABC) transporter. The MetNIQ system is one of the few members of the ABC importer family that has been structurally characterized in multiple conformational states. Critical missing elements in the structural analysis of MetNIQ are the structure of the substrate-free form of MetQ, and detailing how MetQ binds multiple methionine derivatives, including both l- and d-methionine isomers. In this study, we report the structures of the Neisseria meningitides MetQ in substrate-free form and in complexes with l-methionine and with d-methionine, along with the associated binding constants determined by isothermal titration calorimetry. Structures of the substrate-free (N238A) and substrate-bound N. meningitides MetQ are related by a "Venus-fly trap" hinge-type movement of the two domains accompanying methionine binding and dissociation. l- and d-methionine bind to the same site on MetQ, and this study emphasizes the important role of asparagine 238 in ligand binding and affinity. A thermodynamic analysis demonstrates that ligand-free MetQ associates with the ATP-bound form of MetNI ∼40 times more tightly than does liganded MetQ, consistent with the necessity of dissociating methionine from MetQ for transport to occur.
细菌周质甲硫氨酸结合蛋白 MetQ 参与了同型 MetNI 甲硫氨酸 ATP 结合盒(ABC)转运体对甲硫氨酸的摄取。MetNIQ 系统是少数几种在多种构象状态下结构特征得到充分研究的 ABC 导入器家族成员之一。MetNIQ 结构分析中关键缺失的元素是无底物形式的 MetQ 的结构,以及详细说明 MetQ 如何结合多种甲硫氨酸衍生物,包括 l-和 d-甲硫氨酸异构体。在这项研究中,我们报告了脑膜炎奈瑟菌 MetQ 在无底物形式以及与 l-甲硫氨酸和 d-甲硫氨酸复合物中的结构,以及通过等温滴定量热法确定的相关结合常数。无底物(N238A)和底物结合的脑膜炎奈瑟菌 MetQ 结构通过两个结构域的“维纳斯捕蝇草”铰链式运动相关联,伴随着甲硫氨酸的结合和解离。l-和 d-甲硫氨酸结合到 MetQ 的相同位点,本研究强调了天冬酰胺 238 在配体结合和亲和力中的重要作用。热力学分析表明,与结合配体的 MetQ 相比,无配体的 MetQ 与 MetNI 的 ATP 结合形式结合得紧密约 40 倍,这与发生转运需要从 MetQ 上解离甲硫氨酸的必要性一致。