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pcDNA3.1(+)-VEGF165载体的构建及表达蛋白特性分析
引用本文:邱明,肖明朝,苟欣,杨钰兴. pcDNA3.1(+)-VEGF165载体的构建及表达蛋白特性分析[J]. 生物技术通报, 2010, 0(2)
作者姓名:邱明  肖明朝  苟欣  杨钰兴
作者单位:重庆医科大学附属第一医院泌尿外科,重庆,400016
基金项目:重庆市自然科学基金计划项目 
摘    要:构建含人VEGF165基因的重组真核表达质粒,并对其表达蛋白特性进行初步分析。将合成的VEGF165基因序列克隆至pCR2.1-TOPO载体,测序鉴定证实基因碱基序列无误后,再克隆至真核表达载体pcDNA3.1(+),构建成pcD-NA3.1(+)-VEGF165重组质粒。利用DNAstar软件分析基因序列并翻译成氨基酸序列,再用ExPASy protscale和Protean软件分析其疏水特性、蛋白二级结构。经基因测序、酶切鉴定和PCR鉴定证实pcDNA3.1(+)-VEGF165重组质粒构建成功。Ex-PASy protscale和Protean软件分析表明VEGF165蛋白具有较好的水溶性。本研究为VEGF165的基因治疗应用和VEGF165蛋白直接治疗勃起功能障碍奠定了基础。

关 键 词:血管内皮生长因子  基因克隆  序列测定  基因表达

Construction of pcDNA3.1(+)-VEGF165 and Analysis of the Expressed Protein
Qiu Ming,Xiao Mingzhao,Gou Xin,Yang Yuxing. Construction of pcDNA3.1(+)-VEGF165 and Analysis of the Expressed Protein[J]. Biotechnology Bulletin, 2010, 0(2)
Authors:Qiu Ming  Xiao Mingzhao  Gou Xin  Yang Yuxing
Affiliation:Qiu Ming Xiao Mingzhao Gou Xin Yang Yuxing(Department of Urology,the First Affiliated Hospital,Chongqing Medical University,Chongqing 400016)
Abstract:It was to construct the pcDNA3.1(+)-VEGF165 expression vector and analyze the expressed protein.VEGF165 gene was cloned to pCR2.1-TOPO vector and then cloned into the vector pcDNA3.1(+)after sequencing.Two softwares ExPASy protscale and Protean were used to analyze the hydrophobic character and secondary structure of VEGF165 protein.Results indicated that pcDNA3.1(+)-VEGF165 was successfully constructed and confirmed by gene sequencing and PCR identification.Analysis with ExPASy protscale and Protean showed...
Keywords:Vascular endothelial growth factor  Gene cloning  Gene sequencing  Gene expression
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