Werner M H, Gronenborn A M, Clore G M
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0520, USA.
Science. 1996 Feb 9;271(5250):778-84. doi: 10.1126/science.271.5250.778.
Biological processes involved in the control and regulation of transcription are dependent on protein-induced distortions in DNA structure that enhance the recruitment of proteins to their specific DNA targets. This function is often accomplished by accessory factors that bind sequence specifically and locally bend or kink the DNA. The recent determination of the three-dimensional structures of several protein-DNA complexes, involving proteins that perform such architectural tasks, brings to light a common theme of side chain intercalation as a mechanism capable of driving the deformation of the DNA helix. The protein scaffolds orienting the intercalating side chain (or side chains) are structurally diverse, presently comprising four distinct topologies that can accomplish the same task. The intercalating side chain (or side chains), however, is exclusively hydrophobic. Intercalation can either kink or bend the DNA, unstacking one or more adjacent base pairs and locally unwinding the DNA over as much as a full turn of helix. Despite these distortions, the return to B-DNA helical parameters generally occurs within the adjacent half-turns of DNA.
转录控制和调节过程中涉及的生物学过程依赖于蛋白质诱导的DNA结构扭曲,这种扭曲增强了蛋白质与特定DNA靶点的结合。该功能通常由辅助因子完成,这些辅助因子特异性结合序列并使DNA局部弯曲或扭结。最近对几种蛋白质-DNA复合物三维结构的测定揭示了一个共同主题,即侧链插入作为一种能够驱动DNA螺旋变形的机制。引导插入侧链(或多个侧链)的蛋白质支架在结构上多种多样,目前包括四种不同的拓扑结构,它们都能完成相同的任务。然而,插入侧链(或多个侧链)完全是疏水的。插入可使DNA扭结或弯曲,解开一个或多个相邻碱基对,并使DNA局部解旋多达一整圈螺旋。尽管存在这些扭曲,但通常在相邻的半圈DNA内恢复到B-DNA螺旋参数。