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Heterogeneous Subcellular Origin of Exosome-Mimetic Nanovesicles Engineered from Cells.细胞来源的类胞外体纳米囊泡具有异质性的亚细胞起源。
ACS Biomater Sci Eng. 2020 Nov 9;6(11):6063-6068. doi: 10.1021/acsbiomaterials.0c01157. Epub 2020 Oct 29.
2
Chronic exposure to cigarette smoke extract upregulates nicotinic receptor binding in adult and adolescent rats.慢性暴露于香烟烟雾提取物会上调成年和青少年大鼠的烟碱型乙酰胆碱受体结合。
Neuropharmacology. 2020 Dec 15;181:108308. doi: 10.1016/j.neuropharm.2020.108308. Epub 2020 Sep 17.
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Brain Region Specific Single-Molecule Fluorescence Imaging.脑区特异性单分子荧光成像
Anal Chem. 2019 Aug 6;91(15):10125-10131. doi: 10.1021/acs.analchem.9b02133. Epub 2019 Jul 24.
4
Expanding single-molecule fluorescence spectroscopy to capture complexity in biology.拓展单分子荧光光谱技术以捕捉生物学中的复杂性。
Curr Opin Struct Biol. 2019 Oct;58:233-240. doi: 10.1016/j.sbi.2019.05.005. Epub 2019 Jun 15.
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ImageJ2: ImageJ for the next generation of scientific image data.ImageJ2:面向下一代科学图像数据的ImageJ。
BMC Bioinformatics. 2017 Nov 29;18(1):529. doi: 10.1186/s12859-017-1934-z.
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Single-molecule FRET studies of ion channels.离子通道的单分子荧光共振能量转移研究。
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7
Conformational dynamics of an ATP-binding DNA aptamer: a single-molecule study.ATP 结合 DNA 适体的构象动力学:单分子研究。
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8
Whole animal perfusion fixation for rodents.啮齿动物的全动物灌注固定
J Vis Exp. 2012 Jul 30(65):3564. doi: 10.3791/3564.
9
Live-cell imaging of single receptor composition using zero-mode waveguide nanostructures.使用零模波导纳米结构对单个受体组成进行活细胞成像。
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10
Nicotine up-regulates alpha4beta2 nicotinic receptors and ER exit sites via stoichiometry-dependent chaperoning.尼古丁通过依赖于化学计量的伴侣蛋白介导而上调α4β2 型烟碱型乙酰胆碱受体和内质网出口部位。
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来自脑区特异性纳米囊泡的膜受体的单分子研究

Single-Molecule Studies of Membrane Receptors from Brain Region Specific Nanovesicles.

作者信息

Aryal Surya P, Fu Xu, Masud Abdullah A, Neupane Khaga R, Richards Christopher I

机构信息

Department of Chemistry, University of Kentucky, Lexington, Kentucky, USA.

出版信息

Bio Protoc. 2021 May 20;11(10):e4018. doi: 10.21769/BioProtoc.4018.

DOI:10.21769/BioProtoc.4018
PMID:34150925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8187364/
Abstract

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.

摘要

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