Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA.
Structure. 2010 Jan 13;18(1):83-93. doi: 10.1016/j.str.2009.10.014.
High-fidelity DNA polymerases copy DNA rapidly and accurately by adding correct deoxynucleotide triphosphates to a growing primer strand of DNA. Following nucleotide incorporation, a series of conformational changes translocate the DNA substrate by one base pair step, readying the polymerase for the next round of incorporation. Molecular dynamics simulations indicate that the translocation consists globally of a polymerase fingers-opening transition, followed by the DNA displacement and the insertion of the template base into the preinsertion site. They also show that the pyrophosphate release facilitates the opening transition and that the universally conserved Y714 plays a key role in coupling polymerase opening to DNA translocation. The transition involves several metastable intermediates in one of which the O helix is bent in the vicinity of G711. Completion of the translocation appears to require a gating motion of the O1 helix, perhaps facilitated by the presence of G715. These roles are consistent with the high level of conservation of Y714 and the two glycine residues at these positions. It is likely that a corresponding mechanism is applicable to other polymerases.
高保真 DNA 聚合酶通过将正确的脱氧核苷酸三磷酸添加到 DNA 的延伸引物链上来快速、准确地复制 DNA。核苷酸掺入后,一系列构象变化使 DNA 底物按碱基对一步移动,为下一轮掺入做好准备。分子动力学模拟表明,整体上,易位由聚合酶指部张开转变、随后是 DNA 位移以及模板碱基插入预插入位组成。模拟还表明焦磷酸的释放有助于打开转变,并且普遍保守的 Y714 在将聚合酶打开与 DNA 易位偶联中起着关键作用。该转变涉及一个中的几个亚稳态中间物,其中 O 螺旋在 G711 附近弯曲。易位的完成似乎需要 O1 螺旋的门控运动,G715 的存在可能有助于该运动。这些作用与 Y714 和这些位置的两个甘氨酸残基的高度保守性一致。很可能,类似的机制适用于其他聚合酶。