化学
适体
生物素化
辣根过氧化物酶
检出限
分子生物学
噬菌体
噬菌体展示
链霉亲和素
分析物
肽
色谱法
生物化学
生物素
酶
大肠杆菌
生物
基因
作者
Meena Adhikari,Ulrich Strych,Jinsu Kim,Heather Goux,Sagar Dhamane,Mohan‐Vivekanandan Poongavanam,Anna E. V. Hagström,Katerina Kourentzi,Jacinta C. Conrad,Richard C. Willson
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2015-10-12
卷期号:87 (23): 11660-11665
被引量:37
标识
DOI:10.1021/acs.analchem.5b00702
摘要
We introduce the modification of bacteriophage particles with aptamers for use as bioanalytical reporters, and demonstrate the use of these particles in ultrasensitive lateral flow assays. M13 phage displaying an in vivo biotinylatable peptide (AviTag) genetically fused to the phage tail protein pIII were used as reporter particle scaffolds, with biotinylated aptamers attached via avidin-biotin linkages, and horseradish peroxidase (HRP) reporter enzymes covalently attached to the pVIII coat protein. These modified viral nanoparticles were used in immunochromatographic sandwich assays for the direct detection of IgE and of the penicillin-binding protein from Staphylococcus aureus (PBP2a). We also developed an additional lateral flow assay for IgE, in which the analyte is sandwiched between immobilized anti-IgE antibodies and aptamer-bearing reporter phage modified with HRP. The limit of detection of this LFA was 0.13 ng/mL IgE, ∼100 times lower than those of previously reported IgE assays.
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