中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Interaction of Sedlin with chloride intracellular channel proteins

文献类型:期刊论文

作者Fan, LB; Yu, W; Zhu, XL
刊名FEBS LETTERS
出版日期2003
卷号540期号:1页码:77-80
关键词CLIC1 Sedlin TRAPP complex interaction
通讯作者Zhu, XL (reprint author), Chinese Acad Sci, Mol Cell Biol Lab, Inst Biochem & Cell Biol, Shanghai Inst Biol Sci, 320 Yue Yang Rd, Shanghai 200031, Peoples R China.,
英文摘要Sedlin is an evolutionarily conserved protein encoded by the causative gene SEDL for spondyloepiphyseal dysplasia tarda. Nevertheless, how Sedlin mutations cause the disease remains unknown. Here, the intracellular chloride channel protein CLIC1 was shown to associate with Sedlin by yeast two-hybrid screening. Green fluorescence protein-CLIC1 readily coimmunoprecipitated with FLAG-Sedlin. In addition, both proteins colocalized extensively in cytoplasmic vesicular/reticular structures in COS-7 cells, suggesting their interaction at intracellular membranous organelles: Sedlin also associated with CLIC2 in yeast two-hybrid assays. The link between Sedlin and the intracellular chloride channels is the first step to understand their functional interplays. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
学科主题Biochemistry & Molecular Biology ; Biophysics ; Cell Biology
类目[WOS]Biochemistry & Molecular Biology ; Biophysics ; Cell Biology
关键词[WOS]SPONDYLOEPIPHYSEAL DYSPLASIA TARDA ; ION CHANNEL ; VESICLE DOCKING ; CLIC1 NCC27 ; TRAPP ; GENE ; GOLGI ; IDENTIFICATION ; EXPRESSION ; COMPLEX
收录类别SCI
语种英语
WOS记录号WOS:000182146900014
版本出版稿
源URL[http://202.127.25.143/handle/331003/2398]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
推荐引用方式
GB/T 7714
Fan, LB,Yu, W,Zhu, XL. Interaction of Sedlin with chloride intracellular channel proteins[J]. FEBS LETTERS,2003,540(1):77-80.
APA Fan, LB,Yu, W,&Zhu, XL.(2003).Interaction of Sedlin with chloride intracellular channel proteins.FEBS LETTERS,540(1),77-80.
MLA Fan, LB,et al."Interaction of Sedlin with chloride intracellular channel proteins".FEBS LETTERS 540.1(2003):77-80.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

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