Bijvoet Center for Biomolecular Research, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.
Structure. 2012 Apr 4;20(4):667-75. doi: 10.1016/j.str.2012.02.009. Epub 2012 Apr 3.
Human XPF/ERCC1 is a structure-specific DNA endonuclease that nicks the damaged DNA strand at the 5' end during nucleotide excision repair. We determined the structure of the complex of the C-terminal domain of XPF with 10 nt ssDNA. A positively charged region within the second helix of the first HhH motif contacts the ssDNA phosphate backbone. One guanine base is flipped out of register and positioned in a pocket contacting residues from both HhH motifs of XPF. Comparison to other HhH-containing proteins indicates a one-residue deletion in the second HhH motif of XPF that has altered the hairpin conformation, thereby permitting ssDNA interactions. Previous nuclear magnetic resonance studies showed that ERCC1 in the XPF-ERCC1 heterodimer can bind dsDNA. Combining the two observations gives a model that underscores the asymmetry of the human XPF/ERCC1 heterodimer in binding at an ss/ds DNA junction.
人 XPF/ERCC1 是一种结构特异性的 DNA 内切酶,在核苷酸切除修复过程中在 5'端切开受损的 DNA 链。我们确定了 XPF 的 C 末端结构域与 10nt ssDNA 的复合物的结构。第一个 HhH 基序的第二个螺旋内的一个正电荷区域与 ssDNA 磷酸骨架接触。一个鸟嘌呤碱基从碱基对中翻转出来,位于与 XPF 的两个 HhH 基序的残基接触的口袋中。与其他含有 HhH 的蛋白质的比较表明,XPF 的第二个 HhH 基序中缺失了一个残基,改变了发夹构象,从而允许 ssDNA 相互作用。先前的核磁共振研究表明,XPF-ERCC1 异二聚体中的 ERCC1 可以结合 dsDNA。将这两个观察结果结合起来,提出了一个模型,强调了人 XPF/ERCC1 异二聚体在 ss/dsDNA 连接点结合的不对称性。