Cherezov V, Cheng A, Petit J M, Diat O, Caffrey M
Department of Chemistry, Biochemistry and Biophysics Programs, The Ohio State University, Columbus 43210, USA.
Cell Mol Biol (Noisy-le-grand). 2000 Sep;46(6):1133-45.
The call for brighter synchrotron X-radiation sources for use in structural biology research is barely audible as we enter the new millennium. Our brightest sources are already creating havoc when used at design specifications because of radiation damage. The time is long overdue to take stock of where we are and where we wish to go with regards to using existing sources and to designing new ones. The problem of radiation damage is particularly severe in studies involving kinetics and mechanism where cryotechniques are not always viable. Accordingly, we need to understand the very nature of radiation damage and to devise means for minimizing it. This is the thrust of the current study as applied to lipid membranes and mesophases. Here, we report on two very different types of radiation damage. One involves a dramatic phase transformation and the other a disordering of lamellar stacking. How beam energy and dose/rate affect damage is also discussed. The work highlights the nature of the damage process and the need for additional studies if we are to make most efficient use of an important resource, synchrotron radiation.
在我们进入新千年之际,对用于结构生物学研究的更强同步加速器X射线源的呼声几乎难以听闻。由于辐射损伤,我们现有的最强源在按照设计规格使用时就已经造成了严重破坏。早就该对我们在使用现有源以及设计新源方面所处的位置和希望达到的目标进行评估了。在涉及动力学和机理的研究中,辐射损伤问题尤为严重,因为低温技术并非总是可行的。因此,我们需要了解辐射损伤的本质,并想出将其降至最低的方法。这就是当前针对脂质膜和中间相的研究所要探讨的重点。在此,我们报告两种截然不同的辐射损伤类型。一种涉及剧烈的相变,另一种是层状堆积的无序化。还讨论了束流能量以及剂量/速率如何影响损伤。这项工作突出了损伤过程的本质,以及如果我们要最有效地利用同步加速器辐射这一重要资源,就需要进行更多研究。