van der Sleen Lyan, van den Noort Marco, Silbermann Laura-Marie, Poolman Bert, Tych Katarzyna
Department of Biochemistry Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Nijenborgh 3, 9747 AG Groningen, the Netherlands.
Chemical Biology Group, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Nijenborgh 7, 9747 AG Groningen, the Netherlands.
STAR Protoc. 2025 Jun 20;6(2):103869. doi: 10.1016/j.xpro.2025.103869. Epub 2025 Jun 2.
OpuA is an osmoregulatory ATP-binding cassette transporter that undergoes different conformations upon varying salt concentrations and ligand conditions. Here, we present a protocol to study unfolding and interdomain interactions of OpuA using single-molecule optical tweezers (smOT). We describe steps for expression and purification of the protein, lipid nanodisc reconstitution, and sample preparation. We then detail procedures for smOT experiments and data analysis. This protocol also has potential application in the study of interdomain interactions and unfolding of (membrane) proteins in general. For complete details on the use and execution of this protocol, please refer to van der Sleen et al..
OpuA是一种渗透调节性ATP结合盒转运蛋白,在不同盐浓度和配体条件下会发生不同的构象变化。在此,我们展示了一种使用单分子光镊(smOT)研究OpuA的展开和结构域间相互作用的方案。我们描述了蛋白质的表达和纯化、脂质纳米盘重构以及样品制备的步骤。然后,我们详细说明了smOT实验和数据分析的程序。该方案在一般(膜)蛋白的结构域间相互作用和展开研究中也具有潜在应用。有关该方案使用和执行的完整详细信息,请参考范德·斯伦等人的研究。