[Complementarity of microscopies in the structural analysis of DNA minicircles associated to protein MC1].

E Larquet, E Le Cam, A Fourcade, F Culard, P Furrer, E Delain
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Abstract

Electron microscopy of DNA, either free or complexed with ligands, allows the analysis of local conformational variations along individual molecules. Electron microscopy is unique, in that it has the capacity to determine the average behaviour of a population of molecules observed individually, and can thus provide a better appreciation of variability within the series of molecules than biophysical or biochemical methods. Very encouraging results have been obtained by cryoelectron and near-field microscopies, especially atomic force microscopy, in parallel with traditional techniques for visualizing DNA molecules adsorbed onto a support film. Differences in sample processing procedures and image formation modes render these 3 types of microscopies complementary. The torsional stress of a DNA molecule together with a local curvature induced by the protein MC1 from archaebacteria, can be detected within minicircles comprising 207 base pairs.

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[显微镜在MC1蛋白相关DNA微环结构分析中的互补性]。
电子显微镜下的DNA,无论是自由的还是与配体络合的,都可以分析单个分子的局部构象变化。电子显微镜是独一无二的,因为它有能力确定单个观察到的分子群体的平均行为,因此可以比生物物理或生化方法更好地了解分子系列中的变异性。低温电子和近场显微镜,特别是原子力显微镜,已经获得了非常令人鼓舞的结果,与传统技术并行,用于观察吸附在支撑膜上的DNA分子。样品处理程序和图像形成方式的差异使这三种显微镜具有互补性。DNA分子的扭转应力和由来自古细菌的MC1蛋白引起的局部曲率,可以在包含207个碱基对的小环内检测到。
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