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通过假互补肽核酸诱导和调节各向异性DNA弯曲

Inducing and modulating anisotropic DNA bends by pseudocomplementary peptide nucleic acids.

作者信息

Kuhn Heiko, Cherny Dmitry I, Demidov Vadim V, Frank-Kamenetskii Maxim D

机构信息

Center for Advanced Biotechnology and Department of Biomedical Engineering, Boston University, 36 Cummington Street, Boston, MA 02215, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 May 18;101(20):7548-53. doi: 10.1073/pnas.0308756101. Epub 2004 May 10.

Abstract

DNA bending is significant for various DNA functions in the cell. Here, we demonstrate that pseudocomplementary peptide nucleic acids (pcPNAs) represent a class of versatile, sequence-specific DNA-bending agents. The occurrence of anisotropic DNA bends induced by pcPNAs is shown by gel electrophoretic phasing analysis. The magnitude of DNA bending is determined by circular permutation assay and by electron microscopy, with good agreement of calculated mean values between both methods. Binding of a pair of 10-meric pcPNAs to its target DNA sequence results in moderate DNA bending with a mean value of 40-45 degrees, while binding of one self-pc 8-mer PNA to target DNA yields a somewhat larger average value of the induced DNA bend. Both bends are found to be in phase when the pcPNA target sites are separated by distances of half-integer numbers of helical turns of regular duplex DNA, resulting in an enhanced DNA bend with an average value in the range of 80-90 degrees. The occurrence of such a sharp bend within the DNA double helix is confirmed and exploited through efficient formation of 170-bp-long DNA minicircles by means of dimerization of two bent DNA fragments. The pcPNAs offer two main advantages over previously designed classes of nonnatural DNA-bending agents: they have very mild sequence limitations while targeting duplex DNA and they can easily be designed for a chosen target sequence, because their binding obeys the principle of complementarity. We conclude that pcPNAs are promising tools for inducing bends in DNA at virtually any chosen site.

摘要

DNA弯曲对于细胞内的各种DNA功能具有重要意义。在此,我们证明伪互补肽核酸(pcPNA)代表一类通用的、序列特异性的DNA弯曲剂。凝胶电泳相位分析显示了由pcPNA诱导的各向异性DNA弯曲的发生。通过环状置换分析和电子显微镜确定DNA弯曲的程度,两种方法计算的平均值吻合良好。一对10聚体pcPNA与其靶DNA序列结合会导致中等程度的DNA弯曲,平均值为40 - 45度,而一个自身互补的8聚体PNA与靶DNA结合产生的诱导DNA弯曲平均值略大。当pcPNA靶位点被规则双链DNA螺旋圈数的半整数倍距离隔开时,发现两种弯曲同相,导致增强的DNA弯曲,平均值在80 - 90度范围内。通过两个弯曲DNA片段的二聚化有效形成170 bp长的DNA小环,证实并利用了DNA双螺旋内这种急剧弯曲的发生。与先前设计的非天然DNA弯曲剂类别相比,pcPNA具有两个主要优点:它们在靶向双链DNA时序列限制非常温和,并且可以很容易地针对选定的靶序列进行设计,因为它们的结合遵循互补原则。我们得出结论,pcPNA是在几乎任何选定位点诱导DNA弯曲的有前途的工具。

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