Szpotkowski Kamil, Wójcik Klaudia, Kurzyńska-Kokorniak Anna
Department of Ribonucleoprotein Biochemistry, Institute of Bioorganic Chemistry Polish Academy of Sciences, 61-704 Poznan, Poland.
Comput Struct Biotechnol J. 2023 Apr 29;21:2858-2872. doi: 10.1016/j.csbj.2023.04.028. eCollection 2023.
Protein-nucleic acid complexes are involved in all vital processes, including replication, transcription, translation, regulation of gene expression and cell metabolism. Knowledge of the biological functions and molecular mechanisms beyond the activity of the macromolecular complexes can be determined from their tertiary structures. Undoubtably, performing structural studies of protein-nucleic acid complexes is challenging, mainly because these types of complexes are often unstable. In addition, their individual components may display extremely different surface charges, causing the complexes to precipitate at higher concentrations used in many structural studies. Due to the variety of protein-nucleic acid complexes and their different biophysical properties, no simple and universal guideline exists that helps scientists chose a method to successfully determine the structure of a specific protein-nucleic acid complex. In this review, we provide a summary of the following experimental methods, which can be applied to study the structures of protein-nucleic acid complexes: X-ray and neutron crystallography, nuclear magnetic resonance (NMR) spectroscopy, cryogenic electron microscopy (cryo-EM), atomic force microscopy (AFM), small angle scattering (SAS) methods, circular dichroism (CD) and infrared (IR) spectroscopy. Each method is discussed regarding its historical context, advancements over the past decades and recent years, and weaknesses and strengths. When a single method does not provide satisfactory data on the selected protein-nucleic acid complex, a combination of several methods should be considered as a hybrid approach; thus, specific structural problems can be solved when studying protein-nucleic acid complexes.
蛋白质 - 核酸复合物参与所有重要过程,包括复制、转录、翻译、基因表达调控和细胞代谢。通过大分子复合物的三级结构可以确定其活性之外的生物学功能和分子机制。毫无疑问,对蛋白质 - 核酸复合物进行结构研究具有挑战性,主要是因为这类复合物通常不稳定。此外,它们的各个组分可能表现出极其不同的表面电荷,导致复合物在许多结构研究中使用的较高浓度下沉淀。由于蛋白质 - 核酸复合物种类繁多且具有不同的生物物理性质,不存在简单通用的指南来帮助科学家选择一种方法成功确定特定蛋白质 - 核酸复合物的结构。在本综述中,我们总结了以下可用于研究蛋白质 - 核酸复合物结构的实验方法:X射线和中子晶体学、核磁共振(NMR)光谱、低温电子显微镜(cryo - EM)、原子力显微镜(AFM)、小角散射(SAS)方法、圆二色性(CD)和红外(IR)光谱。我们将讨论每种方法的历史背景、过去几十年和近年来的进展以及优缺点。当单一方法无法为所选蛋白质 - 核酸复合物提供令人满意的数据时,应考虑将几种方法结合作为一种混合方法;因此,在研究蛋白质 - 核酸复合物时可以解决特定的结构问题。