DeWalt Emma L, Begue Victoria J, Ronau Judith A, Sullivan Shane Z, Das Chittaranjan, Simpson Garth J
Department of Chemistry, Purdue University, West Lafayette, IN 47907-2084, USA.
Acta Crystallogr D Biol Crystallogr. 2013 Jan;69(Pt 1):74-81. doi: 10.1107/S0907444912042503. Epub 2012 Dec 20.
Polarization-resolved second-harmonic generation (PR-SHG) microscopy is described and applied to identify the presence of multiple crystallographic domains within protein-crystal conglomerates, which was confirmed by synchrotron X-ray diffraction. Principal component analysis (PCA) of PR-SHG images resulted in principal component 2 (PC2) images with areas of contrasting negative and positive values for conglomerated crystals and PC2 images exhibiting uniformly positive or uniformly negative values for single crystals. Qualitative assessment of PC2 images allowed the identification of domains of different internal ordering within protein-crystal samples as well as differentiation between multi-domain conglomerated crystals and single crystals. PR-SHG assessments of crystalline domains were in good agreement with spatially resolved synchrotron X-ray diffraction measurements. These results have implications for improving the productive throughput of protein structure determination through early identification of multi-domain crystals.
描述了偏振分辨二次谐波产生(PR-SHG)显微镜,并将其应用于识别蛋白质晶体聚集体中多个晶体学域的存在,这一点通过同步加速器X射线衍射得到了证实。对PR-SHG图像进行主成分分析(PCA),得到了主成分2(PC2)图像,其中聚集体晶体的区域具有正负对比值,而单晶的PC2图像呈现均匀的正值或均匀的负值。对PC2图像的定性评估能够识别蛋白质晶体样品中不同内部有序性的域,以及区分多域聚集体晶体和单晶。对晶体域的PR-SHG评估与空间分辨同步加速器X射线衍射测量结果高度一致。这些结果对于通过早期识别多域晶体来提高蛋白质结构测定的生产通量具有重要意义。