From the Laboratory of Chemical Physics, NIDDK, National Institutes of Health, Bethesda, Maryland 20892.
From the Laboratory of Chemical Physics, NIDDK, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 2010 Feb 5;285(6):4173-4184. doi: 10.1074/jbc.M109.080937. Epub 2009 Dec 3.
The solution structure of the IIA-IIB complex of the N,N'-diacetylchitobiose (Chb) transporter of the Escherichia coli phosphotransferase system has been solved by NMR. The active site His-89 of IIA(Chb) was mutated to Glu to mimic the phosphorylated state and the active site Cys-10 of IIB(Chb) was substituted by serine to prevent intermolecular disulfide bond formation. Binding is weak with a K(D) of approximately 1.3 mm. The two complementary interaction surfaces are largely hydrophobic, with the protruding active site loop (residues 9-16) of IIB(Chb) buried deep within the active site cleft formed at the interface of two adjacent subunits of the IIA(Chb) trimer. The central hydrophobic portion of the interface is surrounded by a ring of polar and charged residues that provide a relatively small number of electrostatic intermolecular interactions that serve to correctly align the two proteins. The conformation of the active site loop in unphosphorylated IIB(Chb) is inconsistent with the formation of a phosphoryl transition state intermediate because of steric hindrance, especially from the methyl group of Ala-12 of IIB(Chb). Phosphorylation of IIB(Chb) is accompanied by a conformational change within the active site loop such that its path from residues 11-13 follows a mirror-like image relative to that in the unphosphorylated state. This involves a transition of the phi/psi angles of Gly-13 from the right to left alpha-helical region, as well as smaller changes in the backbone torsion angles of Ala-12 and Met-14. The resulting active site conformation is fully compatible with the formation of the His-89-P-Cys-10 phosphoryl transition state without necessitating any change in relative translation or orientation of the two proteins within the complex.
N,N'-二乙酰壳二糖(Chb)转运蛋白的 IIA-IIB 复合物的溶液结构已通过 NMR 解决。将 IIA(Chb)的活性位点 His-89 突变为 Glu 以模拟磷酸化状态,将 IIB(Chb)的活性位点 Cys-10 替换为丝氨酸以防止分子间二硫键形成。结合较弱,K(D)约为 1.3mm。两个互补的相互作用表面主要是疏水性的,突出的 IIB(Chb)活性位点环(残基 9-16)深埋在由两个相邻 IIA(Chb)三聚体亚基界面形成的活性位点裂隙中。界面的中心疏水区被一个极性和带电残基环包围,这些残基提供了相对较少的静电分子间相互作用,这些相互作用有助于正确对齐两个蛋白质。由于空间位阻,尤其是来自 IIB(Chb)的 Ala-12 的甲基,未磷酸化的 IIB(Chb)中的活性位点环的构象与形成磷酰基过渡态中间体不一致。IIB(Chb)的磷酸化伴随着活性位点环内的构象变化,使得其从残基 11-13 的路径相对于未磷酸化状态遵循镜像图像。这涉及 Gly-13 的 phi/psi 角从右到左 alpha 螺旋区域的转变,以及 Ala-12 和 Met-14 的骨架扭转角的较小变化。由此产生的活性位点构象与 His-89-P-Cys-10 磷酰基过渡态的形成完全兼容,而无需在复合物内的两个蛋白质之间改变相对平移或取向。