[1]幸鹏,刘玉琳,喻海琼,等.粉尘螨过敏原脂肪酶的表达、纯化及生物信息学分析[J].江西师范大学学报(自然科学版),2015,(01):101-105.
 XING Peng,LIU Yulin,YU Haiqiong,et al.Prokaryotic Expression,Purification,and Bioinformatics of Lipase, Arecombinant Allergen of Dust Mite[J].Journal of Jiangxi Normal University:Natural Science Edition,2015,(01):101-105.
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粉尘螨过敏原脂肪酶的表达、纯化及生物信息学分析()
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《江西师范大学学报》(自然科学版)[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2015年01期
页码:
101-105
栏目:
出版日期:
2015-02-10

文章信息/Info

Title:
Prokaryotic Expression,Purification,and Bioinformatics of Lipase, Arecombinant Allergen of Dust Mite
作者:
幸鹏;刘玉琳;喻海琼;李盟;刘志刚;刘晓宇
1.深圳大学过敏反应与免疫学研究所,广东 深圳 518060; 2.南昌大学医学院免疫学教研室,江西 南昌 330006
Author(s):
XING PengLIU YulinYU HaiqiongLI MengLIU ZhigangLIU Xiaoyu
关键词:
粉尘螨 过敏原 重组脂肪酶 生物信息学分析
Keywords:
dust mites allergen recombination lipase bioinformatics analysis
分类号:
R 392.11
文献标志码:
A
摘要:
为克隆原核表达并纯化出粉尘螨过敏原脂肪酶蛋白,鉴定其免疫学活性,并分析其分子特征.通过重组合成粉尘螨新过敏原脂肪酶基因,与pET-28a载体连接后转化大肠埃希菌E.coli Top10,用异丙基-β-D-硫代半乳糖苷(IPTG)诱导表达重组新过敏原脂肪酶蛋白; 经镍柱亲和层析纯化出粉尘螨重组脂肪酶蛋白,用Western Blot、ELISA方法检测其免疫原性.用生物信息学软件预测其理化性质、二级结构,并构建分子进化树.成功表达纯化出高纯度的粉尘螨重组脂肪酶蛋白,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)结果显示表达重组产物分子质量约为40 kDa,与理论值一致,纯化后的表达产物经Western blot印迹检测有明显条带显示.信息学分析显示蛋白二级结构由α螺旋(16.38;)、延伸主链(18.93;)、无规则卷曲(64.69;)组成.成功原核表达出粉尘螨过敏原脂肪酶蛋白,并纯化获得较高纯度及较强免疫学活性的重组脂肪酶蛋白,为尘螨过敏性疾病的特异性诊断和免疫治疗奠定理论基础.
Abstract:
To clone,express and purify of dust mite(lipase),test its immunogenicity,and analysis of its structure and function.Synthesize the lipase gene of dust mite,link it to the pET-28a vector,and the recombinant plasmid was transfected into E.coli Top10 and IPTG induces the expression of lipase protein.The protein was purified by nickel-affinity chromatography and its immunological identification was analyzed by Western blot and ELISA.Bioinformatics software were used to predict physicochemical properties,secondary structure and to construct its molecular phylogenetic tree.High purify recombinant lipase protein of dust mite was successful expressed purified.SDS-PAGE results showed that the expression of recombinant allergen was about 40 kDa.After chromatography,the recombinant allergen could band with the serum IgE from patients with asthma in Western Blot.Its secondary structure contained an alpha helix(16.38;),extended strand(18.93;)and random coil(64.69;).The success of prokaryotic expression and of dust mite allergen(lipase),and purified with high purity and strong immunological activity of the recombinant lipase protein.It can lay the foundation for the special diagnosis of allergic diseases.

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相似文献/References:

[1]李钟鸣,邬玉兰,刘志刚.粉尘螨Der f15的基因克隆与其表达载体的构建[J].江西师范大学学报(自然科学版),2013,(02):159.
 LI Zhong-ming,WU Yu-lan,LIU Zhi-gang.Cloning and Vectorconstuction of Der f15 from House Dust Mite Dermatophagoides Farina[J].Journal of Jiangxi Normal University:Natural Science Edition,2013,(01):159.
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备注/Memo

备注/Memo:
国家自然科学基金(31328014,31400786);广东省高等学校国际暨港澳台科技合作创新平台项目(2012gjhz0009);深圳市科技计划国际科技合作项目(GJHZ20130408174112021);深圳市科技计划基础研究项目(JCYJ20130329110735981,JCYJ20120613173233810);深圳市南山区研发项目(KC2012JSYB0003A)
更新日期/Last Update: 1900-01-01