首页> 美国卫生研究院文献>Journal of Biomolecular Techniques : JBT >Generation of Human PTH1R Construct with Flag Epitope Located Internally: Comparison of Two-Fragment Assembly by Using PCR Overlap Extension or Ligase
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Generation of Human PTH1R Construct with Flag Epitope Located Internally: Comparison of Two-Fragment Assembly by Using PCR Overlap Extension or Ligase

机译:带有位于内部的标志表位的人PTH1R构建体的生成:使用PCR重叠延伸或连接酶的两个片段组装的比较

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摘要

Parathyroid hormone (PTH) regulates bone remodeling and calcium and phosphate homeostasis. PTH actions are mediated by type I PTH/PTH-related peptide receptor (PTH1R). There has been no commercially available, specific antibody to detect human PTH1R expression so far. Flag-tagged human PTH1R construct, converting the sequence DKEAPTGS (residues 94–101) in the exon E2 region of PTH1R to DYKDDDDK of Flag epitope, was generated by using PCR overlap extension or ligase enzyme for two-fragment assembly. We found that Flag-tagged PTH1R assembled by ligase was easy to be manipulated, but its efficiency was lower than that of PCR overlap extension. The PTH1R plasmids generated by both techniques were expressed successfully in vitro and in vivo and possessed the same physiological function as wild-type PTH1R. The Flag-tagged PTH1R construct will provide invaluable tools for study of PTH1R signaling and trafficking.
机译:甲状旁腺激素(PTH)调节骨骼重塑以及钙和磷稳态。 PTH作用由I型PTH / PTH相关肽受体(PTH1R)介导。到目前为止,还没有可商购的检测人PTH1R表达的特异性抗体。通过使用PCR重叠延伸或连接酶进行两段组装,生成了标记有标签的人PTH1R构建体,将PTH1R的外显子E2区中的序列DKEAPTGS(94-101位残基)转化为Flag表位的DYKDDDDK。我们发现由连接酶组装的带有Flag标记的PTH1R易于操作,但其效率低于PCR重叠延伸的效率。通过两种技术产生的PTH1R质粒均在体内和体外成功表达,并具有与野生型PTH1R相同的生理功能。带有标志标记的PTH1R构建体将为研究PTH1R信号传导和贩运​​提供宝贵的工具。

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