Hughes S M, Harper G, Brand M D
Biochem Biophys Res Commun. 1984 Jul 18;122(1):56-61. doi: 10.1016/0006-291x(84)90438-8.
Radiation inactivation of rhodopsin in situ using high-energy electrons gave a value for Mr of 20,200 by spectral assay, but 47,100 by assay of rhodopsin regeneration from opsin and 11-cis-retinal (sequence Mr = 38,840). No light/dark differences were seen. We conclude: (a) radiation inactivation measures the size of the functional unit, and the single hit hypothesis does not hold in our experiments; (b) 500 nm absorbance requires only about half the rhodopsin molecule to be intact, but reconstitution of rhodopsin from opsin requires the whole molecule; (c) we find no evidence for functional interactions between rhodopsin monomers in darkness or light.
利用高能电子对视紫红质进行原位辐射失活,通过光谱分析得出视紫红质的相对分子质量(Mr)为20,200,但通过视蛋白和11-顺式视黄醛再生视紫红质的分析得出的Mr为47,100(序列Mr = 38,840)。未观察到光/暗差异。我们得出以下结论:(a)辐射失活测量的是功能单元的大小,单击中假设在我们的实验中不成立;(b)500 nm吸光度仅需要约一半的视紫红质分子保持完整,但从视蛋白重构视紫红质需要整个分子;(c)我们没有发现视紫红质单体在黑暗或光照下存在功能相互作用的证据。