Watanabe Nobuhisa
Division of Biological Sciences, Graduate School of Science, Hokkaido University, Japan.
Acta Crystallogr D Biol Crystallogr. 2006 Aug;62(Pt 8):891-6. doi: 10.1107/S0907444906010432. Epub 2006 Jul 18.
The practical applicability of in-house structure determination using Cr K alpha X-rays (2.29 A) and a loopless free crystal-mounting method was examined using five novel proteins. Proteins from 9.6 to 84 kDa have been solved using this method without any derivatization. In all cases, more than 90% of structures were constructed automatically with side chains by use of the Cr SAD method. The free crystal-mounting technique increases the accuracy of the anomalous differences between Bijvoet mates and makes the in-house single-wavelength SAD method with a Cr K alpha X-ray source a very useful tool for high-throughput structure determination. In addition, a Cr/Cu dual-wavelength system makes it possible to perform structure analysis from phasing to refinement of the structure in-house.
使用五种新型蛋白质研究了利用Cr Kα X射线(2.29 Å)和无环自由晶体安装方法进行内部结构测定的实际适用性。使用该方法已解析出9.6至84 kDa的蛋白质,且无需任何衍生化处理。在所有情况下,超过90%的结构通过使用Cr SAD方法自动构建了侧链。自由晶体安装技术提高了对映体对之间反常差异的准确性,并使具有Cr Kα X射线源的内部单波长SAD方法成为高通量结构测定的非常有用的工具。此外,Cr/Cu双波长系统使得在内部进行从相位分析到结构精修的结构分析成为可能。