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Site-specific labeling of supercoiled DNA

机译:超螺旋DNA的位点特异性标记

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Visualization of site-specific labels in long linear or circular DNA allows unambiguous identification of various local DNA structures. Here we describe a novel and efficient approach to site-specific DNA labeling. The restriction enzyme SfiI binds toDNA but leaves it intact in the presence of calcium and therefore may serve as a protein label of 13 bp recognition sites. Since SfiI requires simultaneous interaction with two DNA recognition sites for stable binding, this requirement is satisfied by providing an isolated recognition site in the DNA target and an additional short DNA duplex also containing the recognition site. The SfiI/DNA complexes were visualized with AFM and the specificity of the labeling was confirmed by the length measurements.Using this approach, two sites in plasmid DNA were labeled in the presence of a large excess of the helper duplex to compete with the formation of looped structures of the intramolecular synaptic complex. We show that the labeling procedure does not interfere with the superhelical tension-driven formation of alternative DNA structures such as cruciforms. The complex is relatively stable at low and high pH (pH 5 and 9) making the developed approach attractive for use at conditions requiring the pH change.
机译:在长线性或环形DNA中可视化位点特异性标记,可以明确鉴定各种局部DNA结构。在这里,我们描述了一种新颖的有效方法来进行位点特异性DNA标记。限制性内切酶SfiI与DNA结合,但在钙的存在下保持完整,因此可以用作13 bp识别位点的蛋白质标记。由于SfiI需要与两个DNA识别位点同时相互作用才能稳定结合,因此可以通过在DNA靶标中提供一个分离的识别位点和一个另外的短DNA双链体来实现此要求,从而满足该要求。用AFM观察SfiI / DNA复合物,并通过长度测量确认标记的特异性。使用这种方法,在大量过量的辅助双链体存在下标记质粒DNA中的两个位点,以竞争形成SfiI / DNA的DNA。分子内突触复合物的环状结构。我们表明,标记程序不会干扰替代DNA结构(如十字形)的超螺旋张力驱动的形成。该复合物在低和高pH值(pH 5和9)下相对稳定,这使得这种开发的方法可用于需要改变pH的条件。

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