2bind GmbH, Regensburg, Germany.
Adv Biochem Eng Biotechnol. 2020;174:1-15. doi: 10.1007/10_2019_103.
Aptamers are single-stranded nucleic acid molecules forming well-defined 3D structures. Aptamers typically bind to their ligands with high affinity and specificity. They are capable of interacting with various kinds of ligands: ions, small molecules, peptides, proteins, viruses, bacteria, and even cells. Therefore, aptamers are in widespread use as sensor molecules or as targeting agents in diagnostics and pharmaceutics. As a prerequisite for their use in these economic high-value areas, aptamers must be studied in detail with respect to different biophysical characteristics. Of central importance are basic binding parameters of the aptamer-target interaction, such as binding affinity and kinetics. Numerous biophysical methods with different features, characteristics, and capabilities are used in the field today for this purpose.This chapter provides an overview of the current state-of-the-art technologies for studying interactions between aptamers and targets and discusses their advantages as well as drawbacks. Furthermore, essential aspects influencing any aptamer characterization strategy will be presented. Finally, issues of comparability of binding data between different aptamer characterization technologies will be discussed. Graphical Abstract.
适配体是形成明确 3D 结构的单链核酸分子。适配体通常与它们的配体具有高亲和力和特异性结合。它们能够与各种配体相互作用:离子、小分子、肽、蛋白质、病毒、细菌,甚至细胞。因此,适配体被广泛用作传感器分子或在诊断学和药剂学中的靶向试剂。作为在这些高经济价值领域中使用的前提条件,必须针对不同的生物物理特性详细研究适配体。核心重要的是适配体-靶相互作用的基本结合参数,例如结合亲和力和动力学。今天,该领域使用了具有不同特点、特性和功能的众多生物物理方法来达到这个目的。本章概述了当前用于研究适配体与靶标相互作用的最新技术,并讨论了它们的优点和缺点。此外,还将介绍影响任何适配体表征策略的重要方面。最后,将讨论不同适配体表征技术之间的结合数据可比性问题。