Zhao M, Zen K C, Hubbell W L, Kaback H R
Howard Hughes Medical Institute, Department of Physiology Molecular Biology Institute, Jules Stein Eye Institute, University of California, Los Angeles, CA, USA.
Biochemistry. 1999 Jun 8;38(23):7407-12. doi: 10.1021/bi9906524.
Evidence has been presented [Venkatesan, P., and Kaback, H. R. (1998) Proc. Natl. Acad. Sci. U.S.A. 95, 9802-9807] that Glu126 (helix IV) and Arg144 (helix V) which are critical for substrate binding in the lactose permease of Escherichia coli are charge paired and therefore in close proximity. To test this conclusion more directly, three different site-directed spectroscopic techniques were applied to permease mutants in which Glu126 and/or Arg144 were replaced with either His or Cys residues. (1) Glu126-->His/Arg144-->His permease containing a biotin acceptor domain was purified by monomeric avidin affinity chromatography, and Mn(II) binding was assessed by electron paramagnetic resonance spectroscopy. The mutant protein binds Mn(II) with a KD of about 40 microM at pH 7.5, while no binding is observed at pH 5.5. In addition, no binding is detected with Glu126-->His or Arg144-->His permease. (2) Permease with Glu126-->Cys/Arg144-->Cys and a biotin acceptor domain was purified, labeled with a thiol-specific nitroxide spin-label, and shown to exhibit spin-spin interactions in the frozen state after reconstitution into proteoliposomes. (3) Glu126-->Cys/Arg144-->Cys permease with a biotin acceptor domain was purified and labeled with a thiol-specific pyrene derivative, and fluorescence spectra were obtained after reconstitution into lipid bilayers. An excimer band is observed with the reconstituted E126C/R144C mutant, but not with either single-Cys mutant or when the single-Cys mutants are mixed prior to reconstitution. The results provide strong support for the conclusion that Glu126 (helix IV) and Arg144 (helix V) are in close physical proximity.
已有证据表明[Venkatesan, P., 和Kaback, H. R. (1998) Proc. Natl. Acad. Sci. U.S.A. 95, 9802 - 9807],大肠杆菌乳糖通透酶中对底物结合至关重要的Glu126(螺旋IV)和Arg144(螺旋V)形成电荷对,因此彼此靠近。为了更直接地验证这一结论,将三种不同的定点光谱技术应用于Glu126和/或Arg144被His或Cys残基取代的通透酶突变体。(1) 含有生物素受体结构域的Glu126→His/Arg144→His通透酶通过单体抗生物素蛋白亲和色谱法纯化,并用电子顺磁共振光谱法评估Mn(II)的结合情况。该突变蛋白在pH 7.5时以约40 μM的KD结合Mn(II),而在pH 5.5时未观察到结合。此外,Glu126→His或Arg144→His通透酶未检测到结合。(2) 含有生物素受体结构域的Glu126→Cys/Arg144→Cys通透酶被纯化,用硫醇特异性氮氧化物自旋标记物标记,并在重构入蛋白脂质体后在冷冻状态下显示出自旋-自旋相互作用。(3) 含有生物素受体结构域的Glu126→Cys/Arg144→Cys通透酶被纯化,并用硫醇特异性芘衍生物标记,在重构入脂质双层后获得荧光光谱。重构后的E126C/R144C突变体观察到准分子带,但单个Cys突变体或重构前混合单个Cys突变体时未观察到。结果为Glu126(螺旋IV)和Arg144(螺旋V)在物理上彼此靠近的结论提供了有力支持。