Debreczeni Judit E, Bunkóczi Gábor, Ma Qingjun, Blaser Heiko, Sheldrick George M
Lehrstuhl für Strukturchemie, Georg-August Universität, Göttingen, Germany.
Acta Crystallogr D Biol Crystallogr. 2003 Apr;59(Pt 4):688-96. doi: 10.1107/s0907444903002646. Epub 2003 Mar 25.
Five test structures (orthorhombic and trigonal trypsin, cubic and rhombohedral insulin and thaumatin) have been solved by the SAD (single-wavelength anomalous diffraction) method using highly redundant data collected at 100 K with a CCD detector, rotating-anode generator and three-circle goniometer. The very weak anomalous scattering (primarily from sulfur) was sufficient to locate all the anomalous scatterers using the integrated direct and Patterson methods in SHELXD. These positions and occupancies were used without further refinement to estimate phases that were extended to native (in-house) resolution by the sphere of influence algorithm in SHELXE. The final map correlation coefficients relative to the anisotropically refined structures were in the range 0.81-0.97. The use of highly redundant medium-resolution laboratory data for sulfur-SAD phasing combined with high-resolution synchrotron native data for phase expansion and structure refinement clearly has considerable potential.
利用电荷耦合器件(CCD)探测器、旋转阳极发生器和三圆测角仪在100 K下收集的高度冗余数据,通过单波长反常散射(SAD)方法解析了五种测试结构(正交和三角晶系的胰蛋白酶、立方和菱面体晶系的胰岛素以及奇异果甜蛋白)。非常微弱的反常散射(主要来自硫)足以使用SHELXD中的直接积分法和帕特森法来定位所有反常散射体。这些位置和占有率未经进一步精修就用于估算相位,然后通过SHELXE中的影响球算法将其扩展到内部原生分辨率。相对于各向异性精修结构的最终图谱相关系数在0.81 - 0.97范围内。将用于硫-SAD相位测定的高度冗余中分辨率实验室数据与用于相位扩展和结构精修的高分辨率同步辐射原生数据相结合,显然具有相当大的潜力。