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由虚拟蛋白引起的DNA弯曲

DNA bending by a phantom protein.

作者信息

Strauss J K, Prakash T P, Roberts C, Switzer C, Maher L J

机构信息

Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, USA.

出版信息

Chem Biol. 1996 Aug;3(8):671-8. doi: 10.1016/s1074-5521(96)90135-0.

Abstract

BACKGROUND

Despite its stiffness, duplex DNA is extensively bent and folded during packaging and gene expression in biological systems. Modulation of the electrostatic repulsion between phosphates in the DNA backbone may be important in the bending of DNA by proteins. Here, we analyze the shape of DNA molecules that have been modified chemically to mimic the electrostatic consequences of a bound protein.

RESULTS

We have simulated salt bridges between DNA phosphates and cationic amino acid sidechains of a phantom protein by tethering ammonium cations to one face of the DNA helix. Tethered ammonium cations, but not neutral acetylated controls, induce DNA to bend toward its neutralized surface.

CONCLUSIONS

The shape of DNA molecules bearing a laterally-asymmetric distribution of tethered cations agrees qualitatively with theoretical predictions and with results previously obtained using neutral phosphate analogs. These data suggest principles that might be applied to the design of artificial DNA-bending proteins.

摘要

背景

尽管双链DNA具有刚性,但在生物系统中的包装和基因表达过程中,它会广泛地弯曲和折叠。调节DNA主链中磷酸根之间的静电排斥力可能对蛋白质使DNA弯曲起重要作用。在此,我们分析了经化学修饰以模拟结合蛋白静电效应的DNA分子的形状。

结果

我们通过将铵阳离子连接到DNA螺旋的一个面上,模拟了DNA磷酸根与虚拟蛋白的阳离子氨基酸侧链之间的盐桥。连接的铵阳离子而非中性乙酰化对照会诱导DNA朝着其被中和的表面弯曲。

结论

带有横向不对称分布连接阳离子的DNA分子形状在定性上与理论预测以及先前使用中性磷酸类似物获得的结果一致。这些数据提示了可能应用于人工DNA弯曲蛋白设计的原理。

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