Main Kavit H S, Provan James I, Haynes Philip J, Wells Geoffrey, Hartley John A, Pyne Alice L B
Institute of Molecular, Cell, and Systems Biology, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
UCL School of Pharmacy, University College London, London WC1N 1AX, United Kingdom.
APL Bioeng. 2021 Jul 9;5(3):031504. doi: 10.1063/5.0054294. eCollection 2021 Sep.
Atomic force microscopy (AFM) is a powerful imaging technique that allows for structural characterization of single biomolecules with nanoscale resolution. AFM has a unique capability to image biological molecules in their native states under physiological conditions without the need for labeling or averaging. DNA has been extensively imaged with AFM from early single-molecule studies of conformational diversity in plasmids, to recent examinations of intramolecular variation between groove depths within an individual DNA molecule. The ability to image dynamic biological interactions has also allowed for the interaction of various proteins and therapeutic ligands with DNA to be evaluated-providing insights into structural assembly, flexibility, and movement. This review provides an overview of how innovation and optimization in AFM imaging have advanced our understanding of DNA structure, mechanics, and interactions. These include studies of the secondary and tertiary structure of DNA, including how these are affected by its interactions with proteins. The broader role of AFM as a tool in translational cancer research is also explored through its use in imaging DNA with key chemotherapeutic ligands, including those currently employed in clinical practice.
原子力显微镜(AFM)是一种强大的成像技术,能够以纳米级分辨率对单个生物分子进行结构表征。AFM具有独特的能力,可在生理条件下对处于天然状态的生物分子进行成像,而无需标记或平均化处理。从早期对质粒构象多样性的单分子研究,到近期对单个DNA分子沟槽深度内分子内变异的研究,DNA已被广泛应用AFM进行成像。对动态生物相互作用进行成像的能力还使得评估各种蛋白质和治疗性配体与DNA的相互作用成为可能,从而深入了解结构组装、灵活性和运动情况。本综述概述了AFM成像的创新与优化如何推进了我们对DNA结构、力学和相互作用的理解。这些研究包括对DNA二级和三级结构的研究,以及其与蛋白质相互作用如何影响这些结构。通过使用AFM对DNA与关键化疗配体(包括目前临床实践中使用的那些)进行成像,还探讨了AFM作为转化癌症研究工具的更广泛作用。