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反式高尔基体网络的一种整合膜蛋白(TGN38)的鉴定、测序及表达

Identification, sequencing and expression of an integral membrane protein of the trans-Golgi network (TGN38).

作者信息

Luzio J P, Brake B, Banting G, Howell K E, Braghetta P, Stanley K K

机构信息

European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.

出版信息

Biochem J. 1990 Aug 15;270(1):97-102. doi: 10.1042/bj2700097.

DOI:10.1042/bj2700097
PMID:2204342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1131683/
Abstract

Organelle-specific integral membrane proteins were identified by a novel strategy which gives rise to monospecific antibodies to these proteins as well as to the cDNA clones encoding them. A cDNA expression library was screened with a polyclonal antiserum raised against Triton X-114-extracted organelle proteins and clones were then grouped using antibodies affinity-purified on individual fusion proteins. The identification, molecular cloning and sequencing are described of a type 1 membrane protein (TGN38) which is located specifically in the trans-Golgi network.

摘要

通过一种新策略鉴定了细胞器特异性整合膜蛋白,该策略可产生针对这些蛋白及其编码cDNA克隆的单特异性抗体。用针对经Triton X - 114提取的细胞器蛋白产生的多克隆抗血清筛选cDNA表达文库,然后使用在单个融合蛋白上亲和纯化的抗体对克隆进行分组。本文描述了一种特异性位于反式高尔基体网络的1型膜蛋白(TGN38)的鉴定、分子克隆和测序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3db4/1131683/d28fa99ac939/biochemj00177-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3db4/1131683/374b43d6e299/biochemj00177-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3db4/1131683/d28fa99ac939/biochemj00177-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3db4/1131683/374b43d6e299/biochemj00177-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3db4/1131683/d28fa99ac939/biochemj00177-0106-a.jpg

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1
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2
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Exp Cell Res. 1983 Mar;144(1):39-46. doi: 10.1016/0014-4827(83)90439-1.
3
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内质网的移动由以Rab-GTP酶为标记的多种囊泡驱动。
Mol Biol Cell. 2025 Jan 1;36(1):ar9. doi: 10.1091/mbc.E24-04-0197. Epub 2024 Dec 4.
4
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Cell Mol Life Sci. 2024 Aug 9;81(1):335. doi: 10.1007/s00018-024-05367-0.
5
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Elife. 2024 Mar 11;12:RP91708. doi: 10.7554/eLife.91708.
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7
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4
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7
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