Department of Biochemistry, Robert Wood Johnson Medical School and Centre for Advanced Biotechnology and Medicine, 679 Hoes Lane, Piscataway, NJ 08854, USA.
Mol Biotechnol. 2011 Mar;47(3):205-10. doi: 10.1007/s12033-010-9330-1.
Gram-negative bacteria consist of two independent membranes, the inner cytoplasmic membrane and the outer membrane. The outer membrane contains a number of β-barrel proteins such as OmpF, OmpC, OmpA, and OmpX. In this article, we explored to use the condensed Single Protein Production (cSPP) system for isotope labelling of OmpA and OmpX for NMR structural study, both of which are known to consist of eight β-strands forming a barrel in the outer membrane. Using a deletion strain lacking all major outer membrane proteins, both OmpA and OmpX were expressed well in a 20-fold cSPP system. We demonstrated that outer membrane fractions prepared from the cSPP system in M9 medium containing ¹⁵N-NH₄Cl can be directly used for NMR structural study of the outer mebrane proteins without any further purification to get excellent [¹H-¹⁵N]-TROSY spectra. This method would be quite valuable for the study of pure proteins in their native membrane environment without the need of purification and reconstitution.
革兰氏阴性菌由两个独立的膜组成,即内膜和外膜。外膜含有许多β-桶状蛋白,如 OmpF、OmpC、OmpA 和 OmpX。在本文中,我们探索了使用浓缩的单蛋白生产 (cSPP) 系统对 OmpA 和 OmpX 进行同位素标记,用于 NMR 结构研究,这两种蛋白都由在外膜中形成桶状结构的八个β-折叠组成。使用缺乏所有主要外膜蛋白的缺失菌株,在 cSPP 系统中以 20 倍的浓度表达 OmpA 和 OmpX。我们证明,在外膜蛋白的 NMR 结构研究中,可以直接使用在含有¹⁵N-NH₄Cl 的 M9 培养基中制备的 cSPP 系统的外膜部分,而无需进一步纯化即可获得出色的[¹H-¹⁵N]-TROSY 谱。这种方法对于在无需纯化和重构的情况下研究天然膜环境中的纯蛋白非常有价值。