HPV16重组减毒沙门氏菌表达质粒的构建及其诱导免疫

VIROLOGICA SINICA(2005)

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Abstract
将人乳头瘤病毒(Human papillomavirus,HPV)16 L1E7基因插入携带霍乱毒素基因的pET-CTA2B载体,获得HPV16L1E7与CTA2B融合表达质粒pET-L1E7CTA2B.在此基础上,通过PCR基因克隆技术,将pET载体的T7启动子与pTETnir15载体的大肠杆菌硝酸盐还原酶基因B启动子nirB进行分割重组,将nirB启动子的厌氧调控元件和启动子基本元件FNR-TATA盒与T7启动子的核糖体结合位点(SD)序列融合,形成nirB-T7杂合启动子.最后获得HPV16重组减毒沙门氏细菌疫苗表达载体pNir-16L1E7CTA2B,并进一步构建对照质粒pNir-16L1E7.Western blot结果证实以上质粒nirB-T7杂合启动子能够在沙门氏细菌中表达L1E7融合蛋白.口服免疫接种小鼠可成功诱导小鼠生殖道产生HPV16特异性粘膜免疫,且霍乱毒素CTA2B可以增强粘膜免疫诱导能力,为开发廉价有效的HPV16预防性疫苗打下了基础.
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Key words
salmonella,hpv16,immunogenicity,recombinant,vivo-inducible
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