Utilizing HaloTag Technology to Track the Fate of PCSK9 from Intracellular vs. Extracellular Sources.

Current chemical genomics Pub Date : 2012-01-01 Epub Date: 2012-09-20 DOI:10.2174/1875397301206010038
Xi Ai, Paul Fischer, Oksana C Palyha, Douglas Wisniewski, Brian Hubbard, Karen Akinsanya, Alison M Strack, Anka G Ehrhardt
{"title":"Utilizing HaloTag Technology to Track the Fate of PCSK9 from Intracellular vs. Extracellular Sources.","authors":"Xi Ai,&nbsp;Paul Fischer,&nbsp;Oksana C Palyha,&nbsp;Douglas Wisniewski,&nbsp;Brian Hubbard,&nbsp;Karen Akinsanya,&nbsp;Alison M Strack,&nbsp;Anka G Ehrhardt","doi":"10.2174/1875397301206010038","DOIUrl":null,"url":null,"abstract":"<p><p>The function of a particular protein is dependent upon its localization and milieu. The ability to track the \"fate\" of a protein is a valuable tool to elucidate its function. We present the use of HaloTag technology to study the localization and fate of human Proprotein Convertase Subtilisin-like Kexin type 9 (PCSK9).The role of PCSK9 in the regulation of circulating low density lipoprotein-cholesterol (LDL-c) levels is ascribed to binding of circulating PCSK9 to the LDL receptor (LDLR) and subsequent lysosomal degradation of LDLR. However, hints in the literature indicate that intracellular PCSK9 may act on the LDLR, possibly during processing of newly synthesized protein. To address this question, the source and fate of intracellular PCSK9 requires further investigation.We applied HaloTag technology to distinguish the source of intracellular PCSK9 and showed that newly synthesized intracellular PCSK9 has unique localization from the PCSK9 after re-uptake. This suggests different functions of PCSK9 while interacting with the LDLR.</p>","PeriodicalId":88232,"journal":{"name":"Current chemical genomics","volume":"6 ","pages":"38-47"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/6c/50/TOCHGENJ-6-38.PMC3480691.pdf","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current chemical genomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1875397301206010038","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/9/20 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7

Abstract

The function of a particular protein is dependent upon its localization and milieu. The ability to track the "fate" of a protein is a valuable tool to elucidate its function. We present the use of HaloTag technology to study the localization and fate of human Proprotein Convertase Subtilisin-like Kexin type 9 (PCSK9).The role of PCSK9 in the regulation of circulating low density lipoprotein-cholesterol (LDL-c) levels is ascribed to binding of circulating PCSK9 to the LDL receptor (LDLR) and subsequent lysosomal degradation of LDLR. However, hints in the literature indicate that intracellular PCSK9 may act on the LDLR, possibly during processing of newly synthesized protein. To address this question, the source and fate of intracellular PCSK9 requires further investigation.We applied HaloTag technology to distinguish the source of intracellular PCSK9 and showed that newly synthesized intracellular PCSK9 has unique localization from the PCSK9 after re-uptake. This suggests different functions of PCSK9 while interacting with the LDLR.

Abstract Image

Abstract Image

Abstract Image

利用HaloTag技术追踪细胞内与细胞外来源PCSK9的命运。
特定蛋白质的功能取决于它的定位和环境。追踪蛋白质“命运”的能力是阐明其功能的宝贵工具。我们利用HaloTag技术研究了人类枯草杆菌样蛋白转化酶(Proprotein Convertase Subtilisin-like Kexin type 9, PCSK9)的定位和命运。PCSK9在循环低密度脂蛋白-胆固醇(LDL-c)水平调控中的作用归因于循环PCSK9与LDL受体(LDLR)的结合以及随后溶酶体对LDLR的降解。然而,文献提示细胞内PCSK9可能作用于LDLR,可能是在新合成蛋白的加工过程中。为了解决这个问题,细胞内PCSK9的来源和命运需要进一步研究。我们利用HaloTag技术区分了细胞内PCSK9的来源,发现新合成的细胞内PCSK9与再摄取后的PCSK9具有独特的定位。这表明PCSK9在与LDLR相互作用时具有不同的功能。
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
×
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