Harbison G S, Herzfeld J, Griffin R G
Biochemistry. 1983 Jan 4;22(1):1-4. doi: 10.1021/bi00270a600.
Solid-state 15N NMR has been employed to examine protonation of the Schiff base linkage in epsilon-[15N]lysylbacteriorhodopsin, the single protein in purple membrane. It is shown with spectra of model compounds that protonation of a Schiff base results in an approximate 150-ppm change in the isotropic 15N chemical shift. Concurrently, the breadth of the shift anisotropy decreases by a factor of about two from 600 to 270 ppm. The isotropic shift of the Schiff base linkage observed in dark-adapted epsilon-[15N]lysylbacteriorhodopsin closely matches those observed for the protonated model compounds, particularly the more weakly hydrogen-bonded ones. It also seems to be affected slightly by isomerization of the retinal.
固态15N核磁共振已被用于研究紫色膜中的单一蛋白质ε-[15N]赖氨酸视紫红质中席夫碱连接的质子化情况。通过模型化合物的光谱表明,席夫碱的质子化导致各向同性15N化学位移发生约150 ppm的变化。同时,位移各向异性的宽度从600 ppm降至270 ppm,减小了约两倍。在暗适应的ε-[15N]赖氨酸视紫红质中观察到的席夫碱连接的各向同性位移与质子化模型化合物观察到的位移紧密匹配,特别是那些氢键较弱的化合物。它似乎也受到视黄醛异构化的轻微影响。