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首页> 外文期刊>Acta crystallographica, Section D. Biological crystallography >Raster-scanning serial protein crystallography using micro- and nano-focused synchrotron beams
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Raster-scanning serial protein crystallography using micro- and nano-focused synchrotron beams

机译:使用微米和纳米聚焦同步加速器束进行光栅扫描系列蛋白质晶体学

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摘要

High-resolution structural information was obtained from lysozyme microcrystals (20 mu m in the largest dimension) using raster-scanning serial protein crystallography on micro- and nano-focused beamlines at the ESRF. Data were collected at room temperature (RT) from crystals sandwiched between two silicon nitride wafers, thereby preventing their drying, while limiting background scattering and sample consumption. In order to identify crystal hits, new multi-processing and GUI-driven Python-based pre-analysis software was developed, named NanoPeakCell, that was able to read data from a variety of crystallographic image formats. Further data processing was carried out using CrystFEL, and the resultant structures were refined to 1.7 angstrom resolution. The data demonstrate the feasibility of RT raster-scanning serial micro- and nano-protein crystallography at synchrotrons and validate it as an alternative approach for the collection of high-resolution structural data from micro-sized crystals. Advantages of the proposed approach are its thriftiness, its handling-free nature, the reduced amount of sample required, the adjustable hit rate, the high indexing rate and the minimization of background scattering.
机译:高分辨率的结构信息是从溶菌酶微晶(最大尺寸为20μm)获得的,该扫描仪使用ESRF在微聚焦和纳米聚焦光束线上进行的光栅扫描系列蛋白质晶体学。在室温(RT)下,从夹在两个氮化硅晶片之间的晶体中收集数据,从而防止其干燥,同时限制了背景散射和样品消耗。为了识别晶体命中,开发了新的多处理和基于GUI的基于Python的预分析软件,名为NanoPeakCell,该软件能够从各种晶体图像格式中读取数据。使用CrystFEL进行进一步的数据处理,并将所得结构精炼到1.7埃分辨率。数据证明了在同步加速器上进行RT光栅扫描串行微和纳米蛋白质晶体学的可行性,并验证了它是从微尺寸晶体中收集高分辨率结构数据的替代方法。所提出的方法的优点是其节俭,免处理性质,减少的所需样品量,可调节的命中率,高指示率和最小的背景散射。

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