期刊文献+

新型冠状病毒N蛋白原核可溶性表达与血清学评价 被引量:3

Prokaryotic Soluble Expression and Serological Evaluation of SARS-CoV-2 N Protein
下载PDF
导出
摘要 目的:利用原核系统可溶性表达新冠病毒(SARS-CoV-2)N蛋白,评价其在血清学诊断上的可行性。方法:将SARS-CoV-2 N蛋白对应的核酸表达序列克隆到载体pET-DsbC上,经原核表达和亲和纯化获得可溶性DsbC-N融合蛋白,通过ELISA试验检测30份确诊新冠肺炎患者、50份健康人血清,评价重组DsbC-N蛋白在新冠肺炎患者血清学诊断中的应用价值。结果:DsbC-N融合蛋白在原核表达系统中以可溶性形式表达,经亲和层析纯化后相对分子质量为68×10^3,纯度为92%。ELISA结果显示纯化后的DsbC-N蛋白与新冠肺炎患者血清有较强的反应,血清学诊断敏感性为96%,特异性为98%。结论:原核可溶性表达的DsbC-N蛋白经纯化后在新冠肺炎诊断方面具有很高的应用价值,可以作为诊断抗原用于检测患者血清中的抗体。 Objective:To prokaryotic express soluble N protein of SARS-CoV-2,and to evaluate its serological diagnosis value.Methods:The nucleicacid sequence of corresponding N protein gene was obtained by PCR and cloned into pET-DsbC vector.After soluble expression and affinity purification,the feasibility was evaluated of fusion protein DsbC-N for clinical serological diagnosis by ELISA with 30 COVID-19 patients and 50 healthy people sera.Results:The DsbC-N fusion protein was expressed in soluble form and efficiently in prokaryotic system with the relative molecular weight was about 68×10^3 and the purity was about 92% after purification by affinity chromatography,which had a significantly higher level of reactivity to sera from COVID-19 patients.The sensitivity and specificity were about 96% and 98% with serological diagnosis.Conclusion:The DsbC-N protein expression in solubity and high purity had an important value in diagnosis of SARS-CoV-2,and might be selected as one of diagnostic antigens to detect antibodies in the serum of COVID-19 patients.
作者 侯江厚 孙卫国 黄国红 詹晓燕 杨奕梅 HOU Jiang-Hou;SUN Wei-Guo;HUANG Guo-Hong;ZHAN Xiao-Yan;YANG Yi-Mei(Kunming City Matermal and Child Health Hospital,Kunming 650013,China;Eighth Medical Center of General Hospital of PLA,Beijing 100091,China)
出处 《生物技术通讯》 CAS 2020年第4期427-431,共5页 Letters in Biotechnology
关键词 新型冠状病毒 N蛋白 可溶性表达 酶联免疫吸附试验 SARS-CoV-2 N protein soluble expression ELISA
  • 相关文献

参考文献3

二级参考文献11

  • 1李伟,杜卫东,张学军.MALDI-TOF MS技术在生物芯片检测中的应用[J].医学分子生物学杂志,2004,1(3):190-193. 被引量:4
  • 2张欣.SARS实验室诊断技术[J].华南预防医学,2004,30(6):75-79. 被引量:2
  • 3冯燕,卢亦愚,严菊英,史雯,李敏红,龚黎明,葛琼,周敏.荧光定量RT-PCR技术快速检测SARS病毒核酸[J].中国病毒学,2005,20(3):228-231. 被引量:24
  • 4钟南山 李兰娟 杨泉森.传染性非典型肺炎[M].杭州:浙江科学技术出版社,2003.36-37.
  • 5Poutanen S M, Low DE, Henry B, et al. Identification of severe acute respiratory syndrome in Canada[J]. N Engl J Med 2003:348,1948-1951.
  • 6Templeton K E, Scheltinga S A, Beersma M F, et al. Rapid and sensitive method using multiplex real-time PCR for diagnosis of infections by influenza a and influenza B viruses, respiratory syncytial virus, and parainfluenza viruses 1, 2, 3, and 4[J]. J Clin Microbiol. 2004. 42(4):1564-1569.
  • 7Stone B, Burrows J, Schepetiuk S,et al. Rapid detection and simultaneous subtype differentiation of influenza A viruses by real time PCR[J]. J Virol Methods. 2004,117(2):103-112.
  • 8Peiris J S. Chu CM, Cheng V C,et al. Clinical progression and viral load in a community outbreak of coronavirus associated SARS pneumonia: a prospective study[J]. Lancet 2003,361:1767-1772.
  • 9Yam W C, Chan K H, Poon L L M.et al. Evaluation of reverse transcription-PCR assays for rapid diagnosis of severe acute respiratory syndrome associated with a novel coronavirus[J]. J Clin Microbiol, 2003,41:4521-4524.
  • 10庄金秋,梅建国,张颖,苗立中,王玉茂.禽流感病毒H7N9亚型实验室检测技术研究进展[J].家禽科学,2019,0(6):53-59. 被引量:5

共引文献605

同被引文献31

引证文献3

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部