...
首页> 外文期刊>Journal of synchrotron radiation >Conformational variation of proteins at room temperature is not dominated by radiation damage
【24h】

Conformational variation of proteins at room temperature is not dominated by radiation damage

机译:室温下蛋白质的构象变化不是辐射损伤的主导

获取原文
获取原文并翻译 | 示例
           

摘要

Protein crystallography data collection at synchrotrons is routinely carried out at cryogenic temperatures to mitigate radiation damage. Although damage still takes place at 100 K and below, the immobilization of free radicals increases the lifetime of the crystals by approximately 100-fold. Recent studies have shown that flash-cooling decreases the heterogeneity of the conformational ensemble and can hide important functional mechanisms from observation. These discoveries have motivated increasing numbers of experiments to be carried out at room temperature. However, the trade-offs between increased risk of radiation damage and increased observation of alternative conformations at room temperature relative to cryogenic temperature have not been examined. A considerable amount of effort has previously been spent studying radiation damage at cryo-temperatures, but the relevance of these studies to room temperature diffraction is not well understood. Here, the effects of radiation damage on the conformational landscapes of three different proteins (T. danielli thaumatin, hen egg-white lysozyme and human cyclophilin A) at room (278 K) and cryogenic (100 K) temperatures are investigated. Increasingly damaged datasets were collected at each temperature, up to a maximum dose of the order of 10(7) Gy at 100 K and 10(5) Gy at 278 K. Although it was not possible to discern a clear trend between damage and multiple conformations at either temperature, it was observed that disorder, monitored by B-factor-dependent crystallographic order parameters, increased with higher absorbed dose for the three proteins at 100 K. At 278 K, however, the total increase in this disorder was only statistically significant for thaumatin. A correlation between specific radiation damage affecting side chains and the amount of disorder was not observed. This analysis suggests that elevated conformational heterogeneity in crystal structures at room temperature is observed despite radiation damage, and not as a result thereof.
机译:同步调节的蛋白质晶体学数据收集在低温温度下进行,以减轻辐射损伤。虽然损伤仍然在100 k及以下发生,但是自由基的固定化将晶体的寿命增加约100倍。最近的研究表明,闪光冷却降低了构象集合的异质性,并可以隐藏观察的重要功能机制。这些发现具有在室温下进行的越来越多的实验。然而,尚未检查辐射损伤风险增加和相对于低温低温在室温下替代构象的增加之间的权衡。先前已经花了大量的努力,以研究冷冻温度的辐射损伤,但这些研究与室温衍射的相关性并不了解。这里,研究了辐射损伤对三种不同蛋白质(T.Danielli Thaumatin,Hen蛋白溶菌酶和人细胞素A)在室内(278k)和低温(100k)温度的效果。在每个温度下收集越来越损坏的数据集,在278 k下,最多10℃的最大剂量为10(7)个GY的10(7)(5)(5)Gy。虽然不可能辨别出损坏和多个之间的明显趋势在任一温度下构造,观察到通过B型依赖性晶体顺序参数监测的病症,随着100k蛋白的三种蛋白质的吸收剂量增加而增加。然而,该疾病的总增加仅是统计学对甲磺汀的重要意义。没有观察到影响侧链的特定辐射损伤与病症的相关性。该分析表明,尽管辐射损坏,但不作为其结果,观察到室温下晶体结构中的构象异质性升高。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号