Hardwidge P R, Den R B, Ross E D, Maher L J
Department of Biochemistry and Molecular Biology, Mayo Foundation, Rochester, MN 55905, USA.
J Biomol Struct Dyn. 2000 Oct;18(2):219-30. doi: 10.1080/07391102.2000.10506660.
Electrophoretic methods are often used to measure DNA curvature and protein-induced DNA bending. Though convenient and widely-applied, quantitative analyses are generally limited to assays for which empirical calibration standards have been developed. Alternatively, solution-based cyclization of short DNA duplexes allows analysis of DNA curvature and bending from first principles, but a detailed understanding of this assay is still lacking. In this work, we demonstrate that calibration with an independent electrophoretic assay of DNA curvature permits interpretation of cyclization assay results in a quantitatively meaningful way. We systematically measure intrinsic DNA curvature in short duplexes using a well-established empirical ligation ladder assay. We then compare the results to those obtained from the analysis of the distribution of circular products obtained in simple enzymatic cyclization assays of the same duplexes when polymerized. A strong correlation between DNA curvature estimates from these two assays is obtained for DNA fragments between 150-300 bp in length. We discuss how this result might be used to improve quantitative analysis of protein-mediated bending events evaluated by cyclization methods. Our results suggest that measurements of DNA curvature obtained under similar conditions, in solution and in an acrylamide gel matrix, can be compared directly. The ability to correlate results of these simple assays may prove convenient in monitoring DNA curvature and flexibility.
电泳方法经常用于测量DNA弯曲度以及蛋白质诱导的DNA弯折。尽管方便且应用广泛,但定量分析通常局限于已开发出经验校准标准的检测方法。另外,短DNA双链体的基于溶液的环化反应能够从第一原理出发分析DNA弯曲度和弯折情况,不过目前对该检测方法仍缺乏详细了解。在这项研究中,我们证明利用一种独立的DNA弯曲度电泳检测进行校准,能够以定量有意义的方式解读环化检测结果。我们使用一种成熟的经验性连接梯检测法系统地测量短双链体中的固有DNA弯曲度。然后,我们将结果与对相同双链体在聚合时进行简单酶促环化检测所获得的环状产物分布分析结果进行比较。对于长度在150 - 300 bp之间的DNA片段,这两种检测方法对DNA弯曲度的估计结果呈现出很强的相关性。我们讨论了该结果如何用于改进通过环化方法评估的蛋白质介导的弯折事件的定量分析。我们的结果表明,在溶液中和丙烯酰胺凝胶基质中相似条件下获得的DNA弯曲度测量结果可以直接进行比较。关联这些简单检测结果的能力可能在监测DNA弯曲度和柔韧性方面被证明是方便的。