Xi Ai, Paul Fischer, Oksana C Palyha, Douglas Wisniewski, Brian Hubbard, Karen Akinsanya, Alison M Strack, Anka G Ehrhardt
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引用次数: 7
摘要
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。
Utilizing HaloTag Technology to Track the Fate of PCSK9 from Intracellular vs. Extracellular Sources.
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.