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本文引用的文献

1
Photoreceptor Phosphodiesterase (PDE6): Structure, Regulatory Mechanisms, and Implications for Treatment of Retinal Diseases.光感受器磷酸二酯酶(PDE6):结构、调控机制及在视网膜疾病治疗中的意义。
Adv Exp Med Biol. 2022;1371:33-59. doi: 10.1007/5584_2021_649.
2
The molecular architecture of photoreceptor phosphodiesterase 6 (PDE6) with activated G protein elucidates the mechanism of visual excitation.光感受器磷酸二酯酶 6(PDE6)与激活的 G 蛋白的分子结构阐明了视觉激发的机制。
J Biol Chem. 2019 Dec 20;294(51):19486-19497. doi: 10.1074/jbc.RA119.011002. Epub 2019 Nov 5.
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Lipid bilayer thickness determines cholesterol's location in model membranes.脂双层厚度决定了胆固醇在模型膜中的位置。
Soft Matter. 2016 Nov 28;12(47):9417-9428. doi: 10.1039/c6sm01777k.
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Supported Lipid Bilayer Technology for the Study of Cellular Interfaces.用于细胞界面研究的支持脂质双层技术
Curr Protoc Cell Biol. 2015 Sep 1;68:24.5.1-24.5.31. doi: 10.1002/0471143030.cb2405s68.
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Silica nanoparticles for the oriented encapsulation of membrane proteins into artificial bilayer lipid membranes.用于将膜蛋白定向包封到人工双层脂质膜中的硅纳米颗粒。
Langmuir. 2015 Mar 3;31(8):2511-6. doi: 10.1021/la504417j. Epub 2015 Feb 20.
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Biomimetic silica microspheres in biosensing.仿生硅微球在生物传感中的应用。
Molecules. 2010 Mar 17;15(3):1932-57. doi: 10.3390/molecules15031932.
7
An overview of lipid membrane supported by colloidal particles.由胶体颗粒支撑的脂质膜概述。
Adv Colloid Interface Sci. 2007 May 31;133(1):1-21. doi: 10.1016/j.cis.2007.02.003. Epub 2007 Feb 28.
8
Structure of fully hydrated fluid phase lipid bilayers with monounsaturated chains.具有单不饱和链的完全水合流体相脂质双层的结构
J Membr Biol. 2005 Dec;208(3):193-202. doi: 10.1007/s00232-005-7006-8. Epub 2006 Apr 8.
9
Purification of PDE6 isozymes from mammalian retina.从哺乳动物视网膜中纯化磷酸二酯酶6同工酶。
Methods Mol Biol. 2005;307:125-40. doi: 10.1385/1-59259-839-0:125.
10
Properties of a self-assembled phospholipid membrane supported on lipobeads.脂质微珠负载的自组装磷脂膜的特性。
Biophys J. 2004 Jul;87(1):323-31. doi: 10.1529/biophysj.103.030627.

G蛋白信号通路膜相关成分在膜包被纳米颗粒(脂质微珠)上的重构。

Reconstitution of Membrane-associated Components of a G-protein Signaling Pathway on Membrane-coated Nanoparticles (Lipobeads).

作者信息

Irwin Michael J, Wang Xin, Cote Rick H

机构信息

Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH 03824, USA.

出版信息

Bio Protoc. 2022 Jan 20;12(2):e4303. doi: 10.21769/BioProtoc.4303.

DOI:10.21769/BioProtoc.4303
PMID:35127993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8799665/
Abstract

G-protein coupled signaling pathways are organized into multi-protein complexes called signalosomes that are located within and on cellular membranes. We describe the use of silica nanoparticles coated with a unilamellar phospholipid bilayer (lipobeads) to reconstitute the activated photoreceptor G-protein α-subunit (Gtα*) with its cognate effector (phosphodiesterase-6; PDE6) for biochemical and structural studies of the activation mechanism regulating this GPCR signaling pathway. Lipobeads are prepared by resuspending dried-down phospholipid mixtures with monodisperse 70 nm silica particles, followed by extrusion through a 100 nm membrane filter. This uniform and supported liposomal preparation is easily sedimented, permitting the separation of soluble from membrane-associated proteins. Upon loading lipobeads with Gtα* and PDE6, we find that activation of PDE6 catalysis by Gtα* occurs much more efficiently than in the absence of membranes. Chemical cross-linking of membrane-confined proteins allows detection of changes in protein-protein interactions, resulting from G-protein activation of PDE6. The advantages of using lipobeads over partially purified membrane preparations or traditional liposomal preparations are generally applicable to the study of other membrane-confined signal transduction pathways.

摘要

G蛋白偶联信号通路被组织成称为信号小体的多蛋白复合物,这些复合物位于细胞膜内和细胞膜上。我们描述了使用包被有单层磷脂双分子层的二氧化硅纳米颗粒(脂质珠)来将活化的光感受器G蛋白α亚基(Gtα*)与其同源效应器(磷酸二酯酶-6;PDE6)进行重组,以用于对调节该GPCR信号通路的激活机制进行生化和结构研究。脂质珠是通过将干燥的磷脂混合物与单分散的70纳米二氧化硅颗粒重悬,然后通过100纳米的膜过滤器挤出而制备的。这种均匀且有支撑的脂质体制剂很容易沉淀,从而可以将可溶性蛋白与膜相关蛋白分离。在用Gtα和PDE6加载脂质珠后,我们发现Gtα对PDE6催化的激活比在没有膜的情况下效率要高得多。对膜限制蛋白进行化学交联可以检测由于PDE6的G蛋白激活而导致的蛋白-蛋白相互作用的变化。与部分纯化的膜制剂或传统脂质体制剂相比,使用脂质珠的优势通常适用于其他膜限制信号转导通路的研究。