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本文引用的文献

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Bridging the Gap between Glycosylation and Vesicle Traffic.连接糖基化与囊泡运输之间的缺口。
Front Cell Dev Biol. 2016 Mar 8;4:15. doi: 10.3389/fcell.2016.00015. eCollection 2016.
2
Dissecting functions of the conserved oligomeric Golgi tethering complex using a cell-free assay.使用无细胞测定法剖析保守寡聚高尔基体连接复合物的功能。
Traffic. 2014 Jan;15(1):12-21. doi: 10.1111/tra.12128. Epub 2013 Oct 31.
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Retrograde vesicle transport in the Golgi.高尔基体内逆行囊泡运输。
Protoplasma. 2012 Oct;249(4):943-55. doi: 10.1007/s00709-011-0361-7. Epub 2011 Dec 12.
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Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.由于保守的寡聚高尔基体复合物亚基 6 的缺乏导致的致死性结局,导致一种新型的先天性糖基化障碍。
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SNARE protein structure and function.SNARE蛋白的结构与功能。
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Isolation of functional Golgi-derived vesicles with a possible role in retrograde transport.分离出可能在逆行运输中起作用的功能性高尔基体衍生囊泡。
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Reconstitution of the transport of protein between successive compartments of the Golgi measured by the coupled incorporation of N-acetylglucosamine.通过 N-乙酰葡糖胺的偶联掺入来测定高尔基体连续区室之间蛋白质转运的重建。
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无细胞荧光高尔基体内逆行囊泡运输测定法

Cell-free Fluorescent Intra-Golgi Retrograde Vesicle Trafficking Assay.

作者信息

Cottam Nathanael P, Ungar Daniel

机构信息

Department of Biology, University of York, York, UK.

出版信息

Bio Protoc. 2017 Nov 20;7(22). doi: 10.21769/BioProtoc.2616.

DOI:10.21769/BioProtoc.2616
PMID:29201946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5706631/
Abstract

Intra-Golgi retrograde vesicle transport is used to traffic and sort resident Golgi enzymes to their appropriate cisternal locations. An assay was established to investigate the molecular details of vesicle targeting in a cell-free system. Stable cell lines were generated in which the -Golgi enzyme galactosyltransferase (GalT) was tagged with either CFP or YFP. Given that GalT is recycled to the cisterna where it is located at steady state, GalT-containing vesicles target GalT-containing cisternal membranes. Golgi membranes were therefore isolated from GalT-CFP expressing cells, while vesicles were prepared from GalT-YFP expressing ones. Incubating CFP-labelled Golgi with YFP-labelled vesicles in the presence of cytosol and an energy regeneration mixture at 37 °C produced a significant increase in CFP-YFP co-localization upon fluorescent imaging of the mixture compared to incubation on ice. The assay was validated to require energy, proteins and physiologically important trafficking components such as Rab GTPases and the conserved oligomeric Golgi tethering complex. This assay is useful for the investigation of both physiological and pathological changes that affect the Golgi trafficking machinery, in particular, vesicle tethering.

摘要

高尔基体内逆行囊泡运输用于将驻留高尔基酶运输并分类到其合适的扁平囊位置。建立了一种检测方法来研究无细胞系统中囊泡靶向的分子细节。构建了稳定细胞系,其中高尔基酶半乳糖基转移酶(GalT)用CFP或YFP进行标记。鉴于GalT在稳态时会循环回到其所在的扁平囊,含GalT的囊泡会靶向含GalT的扁平囊膜。因此,从表达GalT-CFP的细胞中分离高尔基膜,而从表达GalT-YFP的细胞中制备囊泡。与在冰上孵育相比,在37℃下于胞质溶胶和能量再生混合物存在的情况下,将CFP标记的高尔基膜与YFP标记的囊泡一起孵育,对混合物进行荧光成像时,CFP-YFP共定位显著增加。该检测方法经证实需要能量、蛋白质以及生理上重要的运输成分,如Rab GTP酶和保守的寡聚高尔基拴系复合体。该检测方法对于研究影响高尔基运输机制,特别是囊泡拴系的生理和病理变化很有用。