Van Damme Petra
iRIP Unit, Laboratory of Microbiology, Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium.
Methods Mol Biol. 2025;2953:1-16. doi: 10.1007/978-1-0716-4694-6_1.
The delineation of protein-protein interactions through proximity-dependent biotinylation, particularly through the use of biotin ligases such as BioID, has established itself over time as a pivotal method in molecular biology for studying cellular processes in situ. Here, we detail a universally applicable protocol for preparing a diverse array of biological samples for BioID analysis, focusing on the steps from sample isolation to readiness for mass spectrometric analysis. Key steps outlined include mechanical lysis through sonication and freeze-thaw cycles, protein concentration normalization, and the removal of excess biotin through desalting before LC-MS processing. The protocol is designed to standardize sample preparation across diverse biological origins, encompassing a wide array of sample types such as plant tissues, bacterial cultures, and eukaryotic cells or tissues from various species. This adaptability ensures that minimal adjustments are needed for different sample types, thereby standardizing the preparation process to enhance the reliability and comparability of BioID analyses across diverse biological studies.
通过邻近依赖性生物素化,特别是使用诸如BioID之类的生物素连接酶来描绘蛋白质-蛋白质相互作用,随着时间的推移,已成为分子生物学中用于原位研究细胞过程的关键方法。在此,我们详细介绍一种普遍适用的方案,用于制备用于BioID分析的各种生物样品,重点是从样品分离到质谱分析准备就绪的步骤。概述的关键步骤包括通过超声处理和冻融循环进行机械裂解、蛋白质浓度归一化以及在液相色谱-质谱处理之前通过脱盐去除过量的生物素。该方案旨在使来自不同生物学来源的样品制备标准化,涵盖多种样品类型,如植物组织、细菌培养物以及来自各种物种的真核细胞或组织。这种适应性确保了不同样品类型所需的调整最少,从而使制备过程标准化,以提高跨不同生物学研究的BioID分析的可靠性和可比性。