Ullman C G, Haris P I, Galloway D A, Emery V C, Perkins S J
Department of Biochemistry and Molecular Biology, Royal Free Hospital School of Medicine, London, U.K.
Biochem J. 1996 Oct 1;319 ( Pt 1)(Pt 1):229-39. doi: 10.1042/bj3190229.
The E7 and E6 proteins are the main oncoproteins of human papillomavirus types 16 and 18 (HPV-16 and HPV-18), and possess unknown protein structures. E7 interacts with the cellular tumour-suppressor protein pRB and contains a zinc-binding site with two Cys-Xaa2-Cys motifs spaced 29 or 30 residues apart. E6 interacts with another cellular tumour-suppressor protein p53 and contains two zinc-binding sites, each with two Cys-Xaa2-Cys motifs at a similar spacing of 29 or 30 residues. By using the GOR I/III, Chou-Fasman, SAPIENS and PHD methods, the effectiveness of consensus secondary structure predictions on zinc-finger proteins was first tested with sequences for 160 transcription factors and 72 nuclear hormone receptors. These contain Cys2His2 and Cys2Cys2 zinc-binding regions respectively, and possess known atomic structures. Despite the zinc- and DNA-binding properties of these protein folds, the major alpha-helix structures in both zinc-binding regions were correctly identified. Thus validated, the use of these prediction methods with 47 E7 sequences indicated four well-defined alpha-helix (alpha) and beta-sheet (beta) secondary structure elements in the order beta beta alpha beta in the zinc-binding region of E7 at its C-terminus. The prediction was tested by Fourier transform infrared spectroscopy of recombinant HPV-16 E7 in H2O and 2H2O buffers. Quantitative integration showed that E7 contained similar amounts of alpha-helix and beta-sheet structures, in good agreement with the averaged prediction of alpha-helix and beta-sheet structures in E7 and also with previous circular dichroism studies. Protein fold recognition analyses predicted that the structure of the zinc-binding region in E7 was similar to a beta beta alpha beta motif found in the structure of Protein G. This is consistent with the E7 structure predictions, despite the low sequence similarities with E7. This predicted motif is able to position four Cys residues in proximity to a zinc atom. A model for the zinc-binding motif of E7 was constructed by combining the Protein G coordinates with those for the zinc-binding site in transcription factor TFIIS. Similar analyses for the two zinc-binding motifs in E6 showed that they have different alpha/beta secondary structures from that in E7. When compared with 12 other zinc-binding proteins, these results show that E7 and E6 are predicted to possess novel types of zinc-binding structure.
E7和E6蛋白是16型和18型人乳头瘤病毒(HPV - 16和HPV - 18)的主要癌蛋白,其蛋白质结构未知。E7与细胞肿瘤抑制蛋白pRB相互作用,含有一个锌结合位点,该位点有两个间隔29或30个残基的Cys - Xaa2 - Cys基序。E6与另一种细胞肿瘤抑制蛋白p53相互作用,含有两个锌结合位点,每个位点有两个间隔29或30个残基的Cys - Xaa2 - Cys基序。通过使用GOR I/III、Chou - Fasman、SAPIENS和PHD方法,首先用160个转录因子和72个核激素受体的序列测试了锌指蛋白一致性二级结构预测的有效性。这些序列分别包含Cys2His2和Cys2Cys2锌结合区域,并且具有已知的原子结构。尽管这些蛋白质折叠具有锌结合和DNA结合特性,但两个锌结合区域中的主要α - 螺旋结构都被正确识别。经过验证,将这些预测方法用于47个E7序列时,结果表明在E7的C末端锌结合区域中按βββα顺序有四个明确的α - 螺旋(α)和β - 折叠(β)二级结构元件。通过对重组HPV - 16 E7在H2O和2H2O缓冲液中的傅里叶变换红外光谱对该预测进行了测试。定量积分显示E7含有相似数量的α - 螺旋和β - 折叠结构,这与E7中α - 螺旋和β - 折叠结构的平均预测结果以及先前的圆二色性研究结果高度一致。蛋白质折叠识别分析预测E7中锌结合区域的结构类似于蛋白G结构中发现的βββα基序。尽管与E7的序列相似性较低,但这与E7的结构预测结果一致。该预测基序能够使四个半胱氨酸残基靠近一个锌原子。通过将蛋白G的坐标与转录因子TFIIS中锌结合位点的坐标相结合,构建了E7锌结合基序的模型。对E6中两个锌结合基序的类似分析表明,它们具有与E7不同的α/β二级结构。与其他12种锌结合蛋白相比,这些结果表明E7和E6预计具有新型的锌结合结构。