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1
Vesicles on strings: morphological evidence for processive transport within the Golgi stack.串珠状小泡:高尔基体堆栈内进行性运输的形态学证据。
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2279-83. doi: 10.1073/pnas.95.5.2279.
2
A cisternal maturation mechanism can explain the asymmetry of the Golgi stack.潴泡成熟机制可以解释高尔基体堆叠的不对称性。
FEBS Lett. 1997 Sep 8;414(2):177-81. doi: 10.1016/s0014-5793(97)00984-8.
3
A role for giantin in docking COPI vesicles to Golgi membranes.巨糖蛋白在将COPI囊泡对接至高尔基体膜过程中的作用。
J Cell Biol. 1998 Mar 9;140(5):1013-21. doi: 10.1083/jcb.140.5.1013.
4
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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5
Bidirectional transport by distinct populations of COPI-coated vesicles.由不同群体的COPI被膜小泡进行的双向运输。
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Coatomer (COPI)-coated vesicles: role in intracellular transport and protein sorting.衣被蛋白I(COPI)包被小泡:在细胞内运输和蛋白质分选中的作用
Curr Opin Cell Biol. 1997 Aug;9(4):484-7. doi: 10.1016/s0955-0674(97)80023-3.
7
Biogenesis of COPI-coated transport vesicles.COP I 被膜转运小泡的生物发生
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8
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Mechanism of formation of post Golgi vesicles from TGN membranes: Arf-dependent coat assembly and PKC-regulated vesicle scission.源自反式高尔基体网络(TGN)膜的高尔基体后囊泡形成机制:Arf 依赖性衣被组装和蛋白激酶 C(PKC)调节的囊泡切割。
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Purification of a novel class of coated vesicles mediating biosynthetic protein transport through the Golgi stack.一类介导生物合成蛋白通过高尔基体堆叠进行运输的新型被膜小泡的纯化。
Cell. 1989 Jul 28;58(2):329-36. doi: 10.1016/0092-8674(89)90847-7.

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Transport Vesicle Tethering at the Trans Golgi Network: Coiled Coil Proteins in Action.运输小泡在高尔基网络中的锚定:卷曲螺旋蛋白的作用。
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Structural basis for the interaction between the Golgi reassembly-stacking protein GRASP65 and the Golgi matrix protein GM130.高尔基体重新组装-堆叠蛋白GRASP65与高尔基体基质蛋白GM130相互作用的结构基础
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Golgi's way: a long path toward the new paradigm of the intra-Golgi transport.高尔基途径:内高尔基运输新范例的漫漫求索路。
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10
The asymmetrical structure of Golgi apparatus membranes revealed by in situ atomic force microscope.原位原子力显微镜揭示的高尔基器膜的非对称结构。
PLoS One. 2013 Apr 16;8(4):e61596. doi: 10.1371/journal.pone.0061596. Print 2013.

本文引用的文献

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FINE STRUCTURE IN FROZEN-ETCHED YEAST CELLS.酵母细胞的冷冻蚀刻研究
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2
Coupled ER to Golgi transport reconstituted with purified cytosolic proteins.利用纯化的胞质蛋白重建内质网到高尔基体的偶联运输。
J Cell Biol. 1997 Dec 1;139(5):1097-108. doi: 10.1083/jcb.139.5.1097.
3
Bidirectional transport by distinct populations of COPI-coated vesicles.由不同群体的COPI被膜小泡进行的双向运输。
Cell. 1997 Jul 25;90(2):335-49. doi: 10.1016/s0092-8674(00)80341-4.
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Partitioning of the Golgi apparatus during mitosis in living HeLa cells.活的HeLa细胞有丝分裂过程中高尔基体的分割
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5
The vesicle docking protein p115 binds GM130, a cis-Golgi matrix protein, in a mitotically regulated manner.囊泡对接蛋白p115以有丝分裂调节的方式与顺式高尔基体基质蛋白GM130结合。
Cell. 1997 May 2;89(3):445-55. doi: 10.1016/s0092-8674(00)80225-1.
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The production of post-Golgi vesicles requires a protein kinase C-like molecule, but not its phosphorylating activity.高尔基体后囊泡的产生需要一种蛋白激酶C样分子,但并不依赖其磷酸化活性。
J Cell Biol. 1996 Oct;135(2):355-70. doi: 10.1083/jcb.135.2.355.
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Uso1 protein is a dimer with two globular heads and a long coiled-coil tail.Uso1蛋白是一种二聚体,有两个球状头部和一条长的卷曲螺旋尾巴。
J Struct Biol. 1996 May-Jun;116(3):356-65. doi: 10.1006/jsbi.1996.0053.
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Molecular characterization of trans-Golgi p230. A human peripheral membrane protein encoded by a gene on chromosome 6p12-22 contains extensive coiled-coil alpha-helical domains and a granin motif.反式高尔基体p230的分子特征。一种由位于6号染色体p12 - 22区域的基因编码的人类外周膜蛋白,包含广泛的卷曲螺旋α - 螺旋结构域和一个嗜铬粒蛋白基序。
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Assembly of the ER to Golgi SNARE complex requires Uso1p.内质网到高尔基体的SNARE复合体的组装需要Uso1p。
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Coat proteins and vesicle budding.衣被蛋白与囊泡出芽
Science. 1996 Mar 15;271(5255):1526-33. doi: 10.1126/science.271.5255.1526.

串珠状小泡:高尔基体堆栈内进行性运输的形态学证据。

Vesicles on strings: morphological evidence for processive transport within the Golgi stack.

作者信息

Orci L, Perrelet A, Rothman J E

机构信息

Department of Morphology, University of Geneva Medical School, 1211 Geneva 4, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2279-83. doi: 10.1073/pnas.95.5.2279.

DOI:10.1073/pnas.95.5.2279
PMID:9482876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC19319/
Abstract

Cis-Golgi cisternae have a higher freeze-fracture particle density than trans-cisternae. Transport vesicles neighboring cis or trans positions of the Golgi stack have a particle concentration comparable to that of the adjacent cisterna and the buds emerging from it. This implies that transport vesicles remain locally within the stack during their lifetime, near their origin, favoring a processive pattern of transport in which vesicle transfers occur preferentially between adjacent cisternae in the stack. A "string theory" is proposed to account for processive transport, in which a carpet of fibrous attachment proteins located at the surface of cisternae (the strings) prevent budded vesicles from diffusing away but still allow them to diffuse laterally, effectively limiting transfers to adjoining cisternae in the stack. Fibrous elements that multivalently connect otherwise free COPI-coated vesicles and uncoated transport vesicles to one or two cisternae simultaneously are discerned readily by electron microscopy. It is suggested that long, coiled coil, motif-rich, Golgi-specific proteins including p115, GM130, and possibly giantin, among others, function as the proposed strings.

摘要

顺面高尔基体潴泡的冷冻蚀刻颗粒密度高于反面潴泡。靠近高尔基体堆叠顺面或反面位置的运输小泡的颗粒浓度与相邻潴泡及其产生的芽的颗粒浓度相当。这意味着运输小泡在其生命周期内会停留在堆叠内靠近其起源的局部区域,有利于一种连续运输模式,即小泡转移优先发生在堆叠中相邻的潴泡之间。有人提出一种“串理论”来解释连续运输,其中位于潴泡表面的纤维附着蛋白地毯(串)可防止出芽的小泡扩散离开,但仍允许它们横向扩散,从而有效地限制了向堆叠中相邻潴泡的转移。通过电子显微镜很容易识别出多价连接原本游离的COP I被膜小泡和无被运输小泡与一个或两个潴泡的纤维成分。有人认为,包括p115、GM130以及可能还有巨蛋白等在内的长的、富含卷曲螺旋基序的高尔基体特异性蛋白起到了所提出的串的作用。