Aryal Surya P, Fu Xu, Masud Abdullah A, Neupane Khaga R, Richards Christopher I
Department of Chemistry, University of Kentucky, Lexington, Kentucky, USA.
Bio Protoc. 2021 May 20;11(10):e4018. doi: 10.21769/BioProtoc.4018.
Single molecule imaging and spectroscopy are powerful techniques for the study of a wide range of biological processes including protein assembly and trafficking. However, single molecule imaging of biomolecules has been challenging because of difficulties associated with sample preparation and technical challenges associated with isolating single proteins within a biological system. Here we provide a detailed protocol to conduct single molecule imaging where single transmembrane proteins are isolated by rapidly extracting nanovesicles containing receptors of interest from different regions of the brain and subjecting them to single molecule study by using total internal reflection fluorescence (TIRF) microscopy. This protocol discusses the isolation and separation of brain region specific nanovesicles as well as a detailed method to perform TIRF microscopy with those nanovesicles at the single molecule level. This technique can be applied to study trafficking and stoichiometry of various transmembrane proteins from the central nervous system. This approach can be applied to a wide range of animals that are genetically modified to express a membrane protein-fluorescent protein fusion with a wide range of potential applications in many aspects of neurobiology. Graphic abstract: single molecue imaging of membrane receptors.
单分子成像和光谱学是用于研究包括蛋白质组装和运输在内的广泛生物过程的强大技术。然而,生物分子的单分子成像一直具有挑战性,这是因为与样品制备相关的困难以及在生物系统中分离单个蛋白质所涉及的技术挑战。在此,我们提供了一份详细的方案,用于进行单分子成像,即通过从大脑的不同区域快速提取含有感兴趣受体的纳米囊泡来分离单个跨膜蛋白,并使用全内反射荧光(TIRF)显微镜对其进行单分子研究。该方案讨论了脑区特异性纳米囊泡的分离和分选,以及在单分子水平上对这些纳米囊泡进行TIRF显微镜检查的详细方法。这项技术可用于研究来自中枢神经系统的各种跨膜蛋白的运输和化学计量。这种方法可应用于经过基因改造以表达膜蛋白 - 荧光蛋白融合体的多种动物,在神经生物学的许多方面具有广泛的潜在应用。图形摘要:膜受体的单分子成像