Department of Chemistry and Biochemistry, The University of Texas at Dallas, Richardson, TX, USA.
Petit Institute for Bioengineering and Bioscience, School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA, USA.
Methods Mol Biol. 2024;2839:77-97. doi: 10.1007/978-1-0716-4043-2_5.
Transmembrane transition metal transporter proteins are central gatekeepers in selectively controlling vectorial metal cargo uptake and extrusion across cellular membranes in all living organisms, thus playing key roles in essential and toxic metal homeostasis. Biochemical characterization of transporter-mediated translocation events and transport kinetics of redox-active metals, such as iron and copper, is challenged by the complexity in generating reconstituted systems in which vectorial metal transport can be studied in real time. We present fluorescence-based proteoliposome methods to monitor redox-active metal transmembrane translocation upon reconstitution of purified metal transporters in artificial lipid bilayers. By encapsulating turn-on/-off iron or copper-dependent sensors in the proteoliposome lumen and conducting real-time transport assays using small unilamellar vesicles (SUVs), in which selected purified Fe(II) and Cu(I) transmembrane importer and exporter proteins have been reconstituted, we provide a platform to monitor metal translocation events across lipid bilayers in real time. The strategy is modular and expandable toward the study of different transporter families featuring diverse metal substrate selectivity and promiscuity.
跨膜过渡金属转运蛋白是所有生物体中选择性控制载体金属货物摄取和跨细胞膜排出的核心守门员,因此在必需和毒性金属动态平衡中发挥着关键作用。由于在生成可实时研究载体金属运输的重组系统方面存在复杂性,因此对转运蛋白介导的转运事件的生化特征和氧化还原活性金属(如铁和铜)的转运动力学进行了研究。我们提出了基于荧光的蛋白脂体方法,以在纯化金属转运蛋白在人工脂质双层中重组时监测氧化还原活性金属的跨膜转运。通过在蛋白脂体腔中封装开/关型铁或铜依赖性传感器,并使用小单层囊泡(SUV)进行实时转运测定,其中已重建了选定的纯化 Fe(II)和 Cu(I)跨膜输入和输出蛋白,我们提供了一个平台来实时监测脂质双层中金属转运事件。该策略是模块化的,并可扩展到研究具有不同金属底物选择性和混杂性的不同转运蛋白家族。