Forster Marcel C, Tekwani Movellan Kumar, Najbauer Eszter E, Becker Stefan, Andreas Loren B
Department of NMR-based Structural Biology, Max-Planck-Institute for Multidisciplinary Sciences, Am Faßberg 11, 37077 Göttingen, Germany.
J Struct Biol X. 2024 Feb 21;9:100098. doi: 10.1016/j.yjsbx.2024.100098. eCollection 2024 Jun.
Here we report the structure of Opa60 in lipid bilayers using proton-detected magic-angle spinning nuclear magnetic resonance (MAS NMR). Preparations including near-native oligosaccharide lipids reveal a consistent picture of a stable transmembrane beta barrel with a minor increase in the structured region as compared with the previously reported detergent structure. The large variable loops known to interact with host proteins could not be detected, confirming their dynamic nature even in a lipid bilayer environment. The structure provides a starting point for investigation of the functional role of Opa60 in gonococcal infection, which is understood to involve interaction with host proteins. At the same time, it demonstrates the recent advances in proton-detected methodology for membrane protein structure determination at atomic resolution by MAS NMR.
在此,我们使用质子检测魔角旋转核磁共振(MAS NMR)报告了脂质双层中Opa60的结构。包括近天然寡糖脂质在内的制剂揭示了一个稳定的跨膜β桶的一致结构,与先前报道的去污剂结构相比,其结构化区域略有增加。已知与宿主蛋白相互作用的大可变环无法检测到,这证实了它们即使在脂质双层环境中也具有动态性质。该结构为研究Opa60在淋球菌感染中的功能作用提供了一个起点,据了解,这涉及与宿主蛋白的相互作用。同时,它展示了通过MAS NMR在原子分辨率下测定膜蛋白结构的质子检测方法的最新进展。