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慢病毒的超滤浓缩及细胞感染效应
引用本文:郭玲慧,王炜,张岱,张燕,苏航,任伟宏. 慢病毒的超滤浓缩及细胞感染效应[J]. 中国热带医学, 2021, 21(4): 320-324. DOI: 10.13604/j.cnki.46-1064/r.2021.04.04
作者姓名:郭玲慧  王炜  张岱  张燕  苏航  任伟宏
作者单位:1.河南中医药大学,河南 郑州 450046; 2.河南中医药大学第一附属医院检验科,河南 郑州 450000
基金项目:河南省高等学校重点科研项目(No.19zx009)。
摘    要:目的 构建pLVX-CD63-mNeptune-Puro重组质粒,使用HEK293T细胞包装慢病毒,探讨慢病毒经超滤浓缩后的纯化效果极其对MGC-803细胞的转染效应.方法 使用重叠PCR方法构建CD63-mNeptune融合基因,并插入pLVX-Puro载体构建转移质粒.转移质粒、包装质粒和外膜蛋白质粒共转染HEK2...

关 键 词:慢病毒  超滤浓缩  细胞感染  荧光信号
收稿时间:2020-08-05

Ultrafiltration concentration and cell infection of Lentivirus
GUO Ling-hui,WANG Wei,ZHANG Dai,ZHANG Yan,SU Hang,REN Wei-hong. Ultrafiltration concentration and cell infection of Lentivirus[J]. China Tropical Medicine, 2021, 21(4): 320-324. DOI: 10.13604/j.cnki.46-1064/r.2021.04.04
Authors:GUO Ling-hui  WANG Wei  ZHANG Dai  ZHANG Yan  SU Hang  REN Wei-hong
Affiliation:1. He'nan University of Chinese Medicine, Zhengzhou, He'nan 450046, China; 2. Department of Clinical Laboratory, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, He'nan 450000, China
Abstract:Objective To construct the recombinant plasmid pLVX-CD63-mNeptune-Puro,producing Lentivirus in HEK293T cells,and compare the infection efficiency of un-concentrated Lentivirus and ultrafiltration concentrated Lentivirus.Methods The CD63-mNeptune fusion gene was constructed by overlapping PCR.The fusion gene was inserted into the lentiviral expression vector pLVX-Puro to construct the transferred plasmid.Transferred plasmid,packaging plasmid and envelope plasmid were transfected into HEK293T cells.The cell culture medium was collected 48 h and 72 h after transfection.Cell debris and cells in the culture medium are removed by centrifugation at 2500×g for 10 min in 4℃.The supernatant was filtered through a 0.45μm pore PVDF Millex-HV filter(Millipore).The filtrate was collected in a 15 mL centrifuge tube.We took 1 mL of Lentivirus filtrate in a 1.5 mL EP tube.The remaining filtrate was concentrated by using ultrafiltration(with a 100000 cutoff membrane).Then MGC-803 cells were infected with un-concentrated Lentivirus and ultrafiltration concentrated Lentivirus.Efficiency of Lentivirus infection was compared by observing fluorescence signal of MGC-803 cells.ResultsThe Lentivirus transferred plasmid was successfully constructed,and Lentivirus particles were produced by transfection of HEK293T cells.The concentration of lentiviral particles was increased 264 times after ultrafiltration concentration.When cells were infected with the ultrafiltration concentration of Lentivirus,the fluorescence microscopy showed that there were more living cells carrying the fluorescence signal than the un-concentrated Lentivirus.ConclusionThe ultrafiltration concentration method can increase the concentration of virus particles and improve the cell infection efficiency.The method of ultrafiltration to concentrate Lentivirus is suitable for most laboratories.
Keywords:Lentivirus  ultrafiltration concentration  cell infection  fluorescence signal
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