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首页> 外文期刊>World Journal of Gastroenterology >High-yield expression of recpmbinant SARS coronavirus nucleocapsid protein in methylotrophic yeast Pichia pastoris
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High-yield expression of recpmbinant SARS coronavirus nucleocapsid protein in methylotrophic yeast Pichia pastoris

机译:重组SARS冠状病毒核衣壳蛋白在甲基营养酵母毕赤酵母中的高产量表达

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AIM: Nucleocapsid (N) protein plays an important role in reproduction and pathological reaction of severe acute respiratory syndrome (SARS) coronavirus (SCoV), the antigenicity of the protein is better than spike (S) protein. This study was to find a highly specific and antigenic recombinant SCoV nucleocapsid (rSCoVN) protein, and to provide a basis for further researches on early diagnosis of SARS. METHODS: Full length cDNA of SCoV nucleocapsid (SCoVN) protein was amplified through polymerase chain reaction (PCR) and cloned into yeast expression vector pPIC3.5K to construct plasmid of pPIC3.5K-SCoVN. The plasmid was linearized and then transformed into Pichia pastoris (P.pastoris) GS115 (His~- Mut~+) by electroporation. His~+ Mut~+ recombinant strains were identified by PCR and cultivated on MM/MD plates. The influence of different factors on biomass and rSCoVN protein production during induction phase, such as various induction media, dissolved oxygen (DO) and different final concentrations of methanol, was subsequently studied. The expression level and activation were detected by SDS-PAGE and Western-blot respectively. RESULTS: All of the recombinants were His~+ Mut~+ after transformation of P.pastoriswith linearized plasmids. The BMMY medium was optimal for recombinant ScoVN (rSCoVN) protein expression and growth of the recombinant strains. The final optimal concentration of methanol was 20 mL/L, the DO had a significant effect on rSCoVN protein expression and growth of recombinant strains. The rSCoVN protein expressed in recombinant strains was about 8% of the total cell protein, 520 mg/L of rSCoVN protein was achieved, and a maximum cell A at 600 nm of 62 was achieved in shake flask culture. The rSCoVN protein had a high specificity against mouse-anti-SARS-CoVN-mAb and SARS positive sera, but had no cross-reaction with normal human serum. The biological activity of rSCoVN expressed in P.pastoris was about 4-fold higher than that expressed in E. coli when the same rSCoVN protein quantity was used. syndrome (SARS) coronavirus nucleocapsid (rSCoVN) protein can be successfully expressed in recombinant methylotrophic yeast P.pastoris GS115. The rSCoVN protein has a high specificity against SARS-CoVN-mAb and SARS positive sera, but has no cross-reaction with normal human serum. This provides a basis for further researches on the early diagnosis of SARS and the mechanism of SCoV.
机译:目的:核衣壳蛋白(Nucleocapsid(N))在严重急性呼吸综合征(SARS)冠状病毒(SCoV)的繁殖和病理反应中起着重要作用,其抗原性优于穗蛋白(S)。这项研究旨在发现一种高度特异性和抗原性的重组SCoV核衣壳蛋白(rSCoVN),并为进一步研究SARS的早期诊断提供基础。方法:通过聚合酶链反应(PCR)扩增SCoV核衣壳蛋白(SCoVN)的全长cDNA,并将其克隆到酵母表达载体pPIC3.5K中,构建pPIC3.5K-SCoVN质粒。将质粒线性化,然后通过电穿孔转化入巴斯德毕赤酵母(P.pastoris)GS115(His-Mut- +)。通过PCR鉴定His〜+ Mut〜+重组菌株,并在MM / MD平板上培养。随后研究了各种因素对诱导期生物量和rSCoVN蛋白质产生的影响,例如各种诱导培养基,溶解氧(DO)和甲醇终浓度的不同。表达水平和激活分别通过SDS-PAGE和Western-blot检测。结果:用线性化质粒转化枯草芽孢杆菌后,所有重组体均为His〜+ Mut〜+。 BMMY培养基最适合重组ScoVN(rSCoVN)蛋白的表达和重组菌株的生长。甲醇的最终最佳浓度为20 mL / L,DO对rSCoVN蛋白的表达和重组菌株的生长具有显着影响。重组菌株中表达的rSCoVN蛋白约占总细胞蛋白的8%,达到520 mg / L rSCoVN蛋白,摇瓶培养中600 nm处的最大细胞A达到62。 rSCoVN蛋白对小鼠抗SARS-CoVN-mAb和SARS阳性血清具有高度特异性,但与正常人血清无交叉反应。当使用相同数量的rSCoVN蛋白时,在巴斯德毕赤酵母中表达的rSCoVN的生物活性比在大肠杆菌中表达的生物活性高约4倍。综合征(SARS)冠状病毒核衣壳(rSCoVN)蛋白可在重组甲基营养酵母P.pastoris GS115中成功表达。 rSCoVN蛋白对SARS-CoVN-mAb和SARS阳性血清具有很高的特异性,但与正常人血清没有交叉反应。这为进一步研究SARS的早期诊断和SCoV的机制提供了依据。

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