Spooner Paul J R, Sharples Jonathan M, Goodall Scott C, Seedorf Henning, Verhoeven Michiel A, Lugtenburg Johan, Bovee-Geurts Petra H M, DeGrip Willem J, Watts Anthony
The Biomembrane Structure Unit, Department of Biochemistry, University of Oxford, UK.
Biochemistry. 2003 Nov 25;42(46):13371-8. doi: 10.1021/bi0354029.
High-resolution solid-state NMR methods have been used to analyze the conformation of the chromophore in the late photointermediate metarhodopsin-I, from observation of (13)C nuclei introduced into the beta-ionone ring (at the C16, C17, and C18 methyl groups) and into the adjoining segment of the polyene chain (at C8). Bovine rhodopsin in its native membrane was also regenerated with retinal that was (13)C-labeled close to the 11-Z bond (C20 methyl group) to provide a reporter for optimizing and quantifying the photoconversion to metarhodopsin-I. Indirect photoconversion via the primary intermediate, bathorhodopin, was adopted as the preferred method since approximately 44% conversion to the metarhodopsin-I component could be achieved, with only low levels (approximately 18%) of ground-state rhodopsin remaining. The additional photoproduct, isorhodopsin, was resolved in (13)C spectra from C8 in the chain, at levels of approximately 38%, and was shown using rotational resonance NMR to adopt the 6-s-cis conformation between the ring and the polyene chain. The C8 resonance was not shifted in the metarhodopsin-I spectral component but was strongly broadened, revealing that the local conformation had become less well defined in this segment of the chain. This line broadening slowed rotational resonance exchange with the C17 and C18 ring methyl groups but was accounted for to show that, despite the chain being more relaxed in metarhodopsin-I, its average conformation with respect to the ring was similar to that in the ground state protein. Conformational restraints are also retained for the C16 and C17 methyl groups on photoactivation, which, together with the largely preserved conformation in the chain, argues convincingly that the ring remains with strong contacts in its binding pocket prior to activation of the receptor. Previous conclusions based on photocrosslinking studies are considered in view of the current findings.
高分辨率固态核磁共振方法已被用于分析晚期光中间体视紫红质-I中发色团的构象,通过观察引入β-紫罗兰酮环(在C16、C17和C18甲基处)和多烯链相邻片段(在C8处)的(13)C核。天然膜中的牛视紫红质也用在11-Z键(C20甲基)附近进行(13)C标记的视黄醛再生,以提供一个报告分子,用于优化和量化向视紫红质-I的光转化。由于通过初级中间体视紫红质-I可实现约44%的转化,且仅剩余低水平(约18%)的基态视紫红质,因此采用经由初级中间体视紫红质-I的间接光转化作为首选方法。在链中C8处获得的(13)C谱中分辨出了额外的光产物异视紫红质,其含量约为38%,并且利用旋转共振核磁共振表明其在环和多烯链之间采用6-s-顺式构象。视紫红质-I光谱成分中的C8共振未发生位移,但强烈展宽,这表明该链段的局部构象变得不太明确。这种谱线展宽减缓了与C17和C18环甲基的旋转共振交换,但经分析表明,尽管视紫红质-I中的链更松弛,但其相对于环的平均构象与基态蛋白质中的相似。光激活时,C16和C17甲基的构象限制也得以保留,这与链中基本保留的构象一起,令人信服地表明在受体激活之前,环在其结合口袋中仍保持着紧密接触。鉴于当前的研究结果,对基于光交联研究的先前结论进行了重新考量。