摘要
本研究旨在构建人血管性血友病因子裂解蛋白酶(ADAMTS13)的pEGFP-N1真核表达载体,为进一步研究ADAMTS13在细胞内合成及其分泌提供有力工具。通过PCR方法获取目的基因片段,并在目的基因两端加上限制性酶切位点。限制性内切酶酶切后,连接至pEGPF-N1真核表达载体。连接后获得质粒进行酶切鉴定及DNA测序验证,并转染HeLa细胞。通过荧光显微镜检测绿色荧光蛋白表达,Western blot方法鉴定所得蛋白。结果表明,酶切鉴定及DNA测序确认目的基因与载体正确连接,在荧光显微镜下观察到绿色荧光。Western blot显示,转染后HeLa细胞表达ADAMTS13蛋白。结论:成功构建了ADAMTS13-pEGFP-N1真核表达载体,为进一步研究ADAMTS13合成、分泌及其代谢的生理学机制提供了研究工具。
This study was aimed to construct a pEGFP-N1 vector of von Willebrand factor cleaving protease （ADAMTS13, a disintegrin and metalloprotease with a thrombospondin type 1 motifs 13） so as to pave the way for further studing its synthesis and secretion. Human full-length cDNA sequence of ADAMTS13 was acquired by polymerase chain reaction（PCR） with Phusion High-Fidelity（NEB） ,then the PCR product was double digested with EcoR I and XhoⅠ.After digestion, the ADAMTS13 cDNA sequence was purified and recombined with the pEGFP-N1 vector. The DNA sequence analysis showed that ADAMTS13 was ligated to the pEGFP-N1 vector correctly. After transient expression in HeLa cells, the expression of EGFP could be detected by fluorescent microscopy, and the expression of ADAMTS13 protein could be detected by SDS-PAGE and Western blot. It is concluded that the ADAMTS13-pEGFP-N1 vector is successfully constructed, and it can be widely used in further research on the mechanism of the synthesis and secretion of ADAMTS13.
出处
《中国实验血液学杂志》
CAS
CSCD
北大核心
2013年第1期126-129,共4页
Journal of Experimental Hematology
基金
江苏高校优势学科建设工程资助项目
江苏省临床医学中心资助(编号ZX201102)
高等学校博士学科点专项科研基金(编号20103201110011)
