Byrne-Steele Miranda L, Hughes Ronny C, Ng Joseph D
Department of Biological Sciences, University of Alabama in Huntsville, 35899, USA.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Nov 1;65(Pt 11):1131-5. doi: 10.1107/S1744309109037075. Epub 2009 Oct 30.
Proliferating cell nuclear antigen (PCNA) is a DNA-clamping protein that is responsible for increasing the processivity of the replicative polymerases during DNA replication and repair. The PCNA from the eurypsychrophilic archaeon Methanococcoides burtonii DSM 6242 (MbPCNA) has been targeted for protein structural studies. A recombinant expression system has been created that overproduces MbPCNA with an N-terminal hexahistidine affinity tag in Escherichia coli. As a result, recombinant MbPCNA with a molecular mass of 28.3 kDa has been purified to at least 95% homogeneity and crystallized by vapor-diffusion equilibration. Preliminary X-ray analysis revealed a trigonal hexagonal R3 space group, with unit-cell parameters a = b = 102.5, c = 97.5 angstrom. A singleMbPCNA crystal was subjected to complete diffraction data-set collection using synchrotron radiation and reflections were measured to 2.40 angstrom resolution. The diffraction data were of suitable quality for indexing and scaling and an unrefined molecular-replacement solution has been obtained.
增殖细胞核抗原(PCNA)是一种DNA钳夹蛋白,负责在DNA复制和修复过程中提高复制性聚合酶的持续合成能力。嗜冷古菌伯氏甲烷球菌DSM 6242(MbPCNA)的PCNA已被用于蛋白质结构研究。已构建了一种重组表达系统,该系统在大肠杆菌中过量表达带有N端六组氨酸亲和标签的MbPCNA。结果,分子量为28.3 kDa的重组MbPCNA已被纯化至至少95%的纯度,并通过气相扩散平衡法结晶。初步X射线分析显示为三方六方R3空间群,晶胞参数a = b = 102.5,c = 97.5埃。使用同步辐射对单个MbPCNA晶体进行了完整衍射数据集收集,并测量了分辨率为2.40埃的反射。衍射数据质量适合进行指标化和缩放,并且已获得未精制的分子置换解。