Newman Janet, Fazio Vincent J, Caradoc-Davies Tom T, Branson Kim, Peat Thomas S
CSIRO Molecular and Health Technologies, Parkville, VIC, 3052 Australia.
J Biomol Screen. 2009 Dec;14(10):1245-50. doi: 10.1177/1087057109348220.
To provide an experimental basis for a comprehensive molecular modeling evaluation study, 500 fragments from the Maybridge fragment library were soaked into crystals of bovine pancreatic trypsin and the structures determined by X-ray crystallography. The soaking experiments were performed in both single and pooled aliquots to determine if combination of fragments is an appropriate strategy. A further set of data was obtained from co-crystallizing the pooled fragments with the protein. X-ray diffraction data were collected on approximately 1000 crystals at the Australian Synchrotron, and these data were subsequently processed, and the preliminary analysis was performed with a custom software application (Jigsaw), which combines available software packages for structure solution and analysis.
为了给一项全面的分子模型评估研究提供实验依据,将来自Maybridge片段文库的500个片段浸泡到牛胰蛋白酶晶体中,并通过X射线晶体学确定其结构。浸泡实验分别以单个和混合等分试样进行,以确定片段组合是否是一种合适的策略。通过将混合片段与蛋白质共结晶获得了另一组数据。在澳大利亚同步加速器上收集了约1000个晶体的X射线衍射数据,随后对这些数据进行处理,并使用定制软件应用程序(Jigsaw)进行初步分析,该程序结合了用于结构解析和分析的现有软件包。