Department of Biochemistry and Molecular Genetics, School of Medicine, University of Colorado Denver, School of Medicine, Aurora, Colorado.
Mucosal and Vaccine Research Program Colorado (MAVRC) & Denver Veterans Affairs Medical Center, Aurora, Colorado.
Protein Sci. 2019 Oct;28(10):1797-1805. doi: 10.1002/pro.3693. Epub 2019 Aug 9.
Many bacterial pathogens express small G5 domains that exist in the context of various membrane-anchored proteins and these G5 domains have been associated with colonization, cellular adhesion, and biofilm formation. However, despite over a decade since the computational prediction of these G5 domains, many remain uncharacterized, particularly those from Streptococcus pneumoniae. Of five previously predicted G5 domains we found that four of these, all derived from S. pneumoniae, are independently folded modules. As one of these exhibits extreme line broadening due to self-association, we were able to use NMR solution studies to probe the potential ligand interactions of the remaining three G5 domains. None of these G5 domains engage N-acetylglucosamine (NAG) as previously predicted but do interact with other small molecules that may modulate adherence to both bacteria and host cells. Specifically, while all G5 domains tested engage Zn, only one of these G5 domains engage heparin. NMR solution structural studies of the IgA1 Protease G5 (IgA1P-G5) and endo-beta-N-acetylglucosaminidase-D G5 (ENDD-G5) also facilitated identification of the ligand binding sites and confirm the typical G5 fold that comprises two connected β-sheets with no canonical core. NMR relaxation experiments indicate flexibility on both ends and within the connecting regions between the β-sheets. Our studies thus establish a basis for future biological experiments to test whether the ligands presented here are involved in bacterial adherence, either to bacteria or to host cells.
许多细菌病原体表达存在于各种膜锚定蛋白中的小 G5 结构域,这些 G5 结构域与定植、细胞黏附和生物膜形成有关。然而,尽管自这些 G5 结构域的计算预测以来已经过去了十多年,但许多 G5 结构域仍然没有被表征,特别是来自肺炎链球菌的 G5 结构域。在之前预测的五个 G5 结构域中,我们发现其中四个,全部来自肺炎链球菌,是独立折叠的模块。由于其中一个由于自缔合而表现出极端的线宽增宽,我们能够使用 NMR 溶液研究来探测其余三个 G5 结构域的潜在配体相互作用。这些 G5 结构域都没有像之前预测的那样与 N-乙酰葡萄糖胺 (NAG) 结合,但确实与其他可能调节与细菌和宿主细胞黏附的小分子相互作用。具体而言,虽然所有测试的 G5 结构域都与 Zn 结合,但其中只有一个 G5 结构域与肝素结合。IgA1 蛋白酶 G5 (IgA1P-G5) 和内-β-N-乙酰氨基葡萄糖苷酶-D G5 (ENDD-G5) 的 NMR 溶液结构研究还促进了配体结合位点的鉴定,并证实了典型的 G5 折叠,由两个连接的 β-片层组成,没有典型的核心。NMR 弛豫实验表明在β-片层的两端和连接区域内都具有灵活性。因此,我们的研究为未来的生物学实验奠定了基础,以测试这里呈现的配体是否参与细菌黏附,无论是与细菌还是与宿主细胞的黏附。