Tateno M, Yamasaki K, Amano N, Kakinuma J, Koike H, Allen M D, Suzuki M
AIST-NIBHT CREST Centre of Structural Biology, Tsukuba, Japan.
Biopolymers. 1997;44(4):335-59. doi: 10.1002/(SICI)1097-0282(1997)44:4<335::AID-BIP3>3.0.CO;2-R.
The modes of DNA recognition by beta-sheets are analyzed by using the known crystal and solution three-dimensional structures of DNA-protein complexes. Close fitting of the protein surface and the DNA surface determines the binding geometry. Interaction takes place so that essentially the N-to-C direction of the beta-strands either follows or crosses the DNA groove. Upon following the major groove a two-stranded antiparallel beta-sheet dives into the groove and contacts DNA bases with its convex side facing the DNA, while upon following the minor groove, it binds around the sugar-phosphate backbones, with its opposite concave side shielding the DNA. In order for the beta-strands crossing the minor groove to interact with the DNA, the dinucleotide steps need to almost totally helically untwist and roll around major groove. The beta-sheet, on the other hand, needs to adopt a concave curvature on the binding surface in the direction that follows the DNA minor groove, and a convex surface in the direction that bridges the sugar-phosphate backbones across the groove. The result is to produce a hyperbolic paraboloidal DNA-binding surface.
通过使用已知的DNA-蛋白质复合物晶体结构和溶液三维结构,分析了β折叠对DNA的识别模式。蛋白质表面与DNA表面的紧密贴合决定了结合几何形状。相互作用发生的方式是,β链基本上从N端到C端的方向要么沿着DNA沟,要么穿过DNA沟。沿着大沟时,一个双链反平行β折叠潜入沟中,其凸面朝向DNA与DNA碱基接触;而沿着小沟时,它围绕磷酸核糖骨架结合,其相对的凹面屏蔽DNA。为了使穿过小沟的β链与DNA相互作用,二核苷酸步需要几乎完全螺旋解旋并围绕大沟滚动。另一方面,β折叠需要在沿着DNA小沟的方向上在结合表面形成凹曲率,在跨越沟连接磷酸核糖骨架的方向上形成凸表面。结果是产生一个双曲抛物面的DNA结合表面。