Nanao Max H, Ravelli Raimond B G
European Molecular Biology Laboratory (EMBL), Grenoble Outstation, 6 rue Jules Horowitz, B.P. 181, 38042 Grenoble Cedex 9, France.
Structure. 2006 Apr;14(4):791-800. doi: 10.1016/j.str.2006.02.007.
Experimental phasing of macromolecular crystal structures relies on the accurate measurement of two or more sets of reflections from isomorphous crystals, where the scattering power of a few atoms is different for each set. Recently, it was demonstrated that X-ray-induced intensity differences can also contain phasing information, exploiting specific structural changes characteristic of X-ray damage. This method (radiation damage-induced phasing; RIP) has the advantage that it can be performed on a single crystal of the native macromolecule. However, a drawback is that X-rays introduce many small changes to both solvent and macromolecule. In this study, ultraviolet (UV) radiation has been used to induce specific changes in the macromolecule alone, leading to a larger contrast between radiation-susceptible and nonsusceptible sites. Unlike X-ray RIP, UV RIP does not require the use of a synchrotron. The method has been demonstrated for a series of macromolecules.
大分子晶体结构的实验相位分析依赖于对来自同晶型晶体的两组或更多组反射的精确测量,其中每组中少数原子的散射能力不同。最近,有人证明X射线诱导的强度差异也可以包含相位信息,利用X射线损伤特有的特定结构变化。这种方法(辐射损伤诱导相位分析;RIP)的优点是可以在天然大分子的单晶上进行。然而,一个缺点是X射线会对溶剂和大分子都引入许多小的变化。在本研究中,紫外线(UV)辐射已被用于仅在大分子中诱导特定变化,从而导致辐射敏感位点和非敏感位点之间的对比度更大。与X射线RIP不同,UV RIP不需要使用同步加速器。该方法已在一系列大分子上得到验证。