Quantitative electron microscopic analysis of DNA-protein interactions.

E Le Cam, B Théveny, B Mignotte, B Révet, E Delain
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引用次数: 18

Abstract

Electron microscopy offers a unique potentiality to visualize individual molecules. For the last 30 years it has been used to study the structure and the interactions of various biological macromolecules. The contribution of electron microscopy is important because of its capacity to demonstrate the existence of conformational structures such as kinks, bents, loops, etc., either on naked DNA, or on DNA associated with various proteins or ligands. Increasing interest was given to such observations when it was found that they provide a direct visualization of interacting molecules involved in DNA metabolism and gene regulation. Technical advances in the preparation of the specimens, their observation in the electron microscope, and the image processing by computers have allowed the shifting from qualitative to quantitative analysis, as illustrated by a few examples from our laboratory.

dna -蛋白质相互作用的定量电镜分析。
电子显微镜为观察单个分子提供了独特的潜力。在过去的30年里,它被用于研究各种生物大分子的结构和相互作用。电子显微镜的贡献是重要的,因为它能够证明在裸DNA上或在与各种蛋白质或配体相关的DNA上存在构象结构,如扭结、弯曲、环等。当发现它们提供了参与DNA代谢和基因调控的相互作用分子的直接可视化时,人们对这些观察结果的兴趣越来越大。在标本制备、电子显微镜观察和计算机图像处理方面的技术进步,已经使定性分析向定量分析转变,正如我们实验室的几个例子所说明的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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