School of Biosciences, University of Kent, Canterbury, UK.
Methods Mol Biol. 2022;2476:129-143. doi: 10.1007/978-1-0716-2221-6_10.
Many protein interactions with DNA are reliant on the presence of specific DNA sequences, adducts, or structures. In bulk-phase experiments such DNA features are facile to include in a study. For single-molecule imaging this can be more difficult, because the constraints of the assay limit the variety of adducts that can be used. Surface-immobilized DNA provides an ideal compromise, and the use of interferometric scattering microscopy allows for high-speed imaging of these interactions. Furthermore, this technique offers the ability to identify binder stoichiometry and the composition of protein complexes. Its implementation is relatively simple; however data analysis and deconvolution are more challenging. In this chapter we examine how this technique is implemented and reveal software that can be used to deconvolute the images. Altogether, we hope to make this technique more accessible for studying specific DNA-protein interactions on tailored substrates.
许多与 DNA 的蛋白质相互作用依赖于特定的 DNA 序列、加合物或结构的存在。在批量实验中,这些 DNA 特征很容易包含在研究中。对于单分子成像来说,这可能更加困难,因为测定的限制限制了可以使用的加合物的种类。表面固定化 DNA 提供了一个理想的折衷方案,而干涉散射显微镜的使用允许对这些相互作用进行高速成像。此外,该技术还能够识别配体计量和蛋白质复合物的组成。它的实现相对简单;然而,数据分析和解卷积更加具有挑战性。在本章中,我们研究了如何实现该技术,并揭示了可用于解卷积图像的软件。总的来说,我们希望使这项技术更容易用于在定制衬底上研究特定的 DNA-蛋白质相互作用。