[Identification of interaction and interaction domains between neuroglobin and Na(+), K(+)-ATPase beta2 subunit].

Wen-Lin Xu, Chun-Li Wang, Zhi-Yong Liao, Yong-Liang Zhang, Li-Hong Yu, Fan-Wei Meng, Xin-Xing Wang, Fan-Wei Meng, Zhao-Yun Yin, Ling-Jia Qian, Cheng-Gang Zhang
{"title":"[Identification of interaction and interaction domains between neuroglobin and Na(+), K(+)-ATPase beta2 subunit].","authors":"Wen-Lin Xu,&nbsp;Chun-Li Wang,&nbsp;Zhi-Yong Liao,&nbsp;Yong-Liang Zhang,&nbsp;Li-Hong Yu,&nbsp;Fan-Wei Meng,&nbsp;Xin-Xing Wang,&nbsp;Fan-Wei Meng,&nbsp;Zhao-Yun Yin,&nbsp;Ling-Jia Qian,&nbsp;Cheng-Gang Zhang","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The pre-transformed human fetal brain cDNA library was used to screen the protein interacting with neuroglobin by using yeast two hybrid system III from ClonTech Inc. The protein encoded by one of the clones interacting with neuroglobin (NGB) was confirmed to be the C terminus of the Na(+), K(+)-ATPase beta2 subunit (NKA1b2) based on amino acid sequences. Then the full-length coding region cDNA sequence of NKA1b2 was obtained from human fetal brain cDNA library by PCR. A set of experiments were designed to test the interaction between NGB and NKA1b2. Interaction between NGB and NKA1b2 was confirmed by binding assay in vitro. Furthermore, the interaction was also proved by co-immunoprecipitation test in vivo. Moreover, the structure integrity of neuroglobin was found to be essential for the interaction between NGB and NKA1b2 by yeast two hybrid method with a series of neuroglobin truncated mutants.</p>","PeriodicalId":21763,"journal":{"name":"Sheng wu hua xue yu sheng wu wu li xue bao Acta biochimica et biophysica Sinica","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2003-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sheng wu hua xue yu sheng wu wu li xue bao Acta biochimica et biophysica Sinica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The pre-transformed human fetal brain cDNA library was used to screen the protein interacting with neuroglobin by using yeast two hybrid system III from ClonTech Inc. The protein encoded by one of the clones interacting with neuroglobin (NGB) was confirmed to be the C terminus of the Na(+), K(+)-ATPase beta2 subunit (NKA1b2) based on amino acid sequences. Then the full-length coding region cDNA sequence of NKA1b2 was obtained from human fetal brain cDNA library by PCR. A set of experiments were designed to test the interaction between NGB and NKA1b2. Interaction between NGB and NKA1b2 was confirmed by binding assay in vitro. Furthermore, the interaction was also proved by co-immunoprecipitation test in vivo. Moreover, the structure integrity of neuroglobin was found to be essential for the interaction between NGB and NKA1b2 by yeast two hybrid method with a series of neuroglobin truncated mutants.

[神经球蛋白与Na(+), K(+)- atp酶β 2亚基的相互作用和相互作用域的鉴定]。
利用克隆科技公司(ClonTech Inc.)的酵母双杂交系统III,利用预转化的人胎儿大脑cDNA文库筛选与神经球蛋白相互作用的蛋白。其中一个与神经球蛋白(NGB)相互作用的克隆编码的蛋白根据氨基酸序列确定为Na(+), K(+)- atp酶β 2亚基(NKA1b2)的C端。利用PCR方法从人胎脑cDNA文库中获得NKA1b2全长编码区cDNA序列。设计了一套实验来测试NGB与NKA1b2之间的相互作用。体外结合实验证实NGB与NKA1b2之间存在相互作用。此外,体内共免疫沉淀试验也证实了相互作用。此外,通过酵母双杂交方法和一系列神经红蛋白截断突变体发现,神经红蛋白的结构完整性是NGB和NKA1b2相互作用的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
文献相关原料
公司名称 产品信息 采购帮参考价格
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信