Ulrich Strych - Academia.edu (original) (raw)

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Papers by Ulrich Strych

Research paper thumbnail of Detection of viruses by counting single fluorescent genetically biotinylated reporter immunophage using a lateral flow assay

ACS applied materials & interfaces, Jan 4, 2015

We demonstrated a lateral flow immunoassay (LFA) for detection of viruses using fluorescently lab... more We demonstrated a lateral flow immunoassay (LFA) for detection of viruses using fluorescently labeled M13 bacteriophage as reporters and single-reporter counting as the readout. AviTag-biotinylated M13 phage were functionalized with antibodies using avidin-biotin conjugation and fluorescently labeled with AlexaFluor 555. Individual phage bound to target viruses (here MS2 as a model) captured on an LFA membrane strip were imaged using epi-fluorescence microscopy. Using automated image processing, we counted the number of bound phage in micrographs as a function of target concentration. The resultant assay was more sensitive than enzyme-linked immunosorbent assays and traditional colloidal-gold nanoparticle LFAs for direct detection of viruses.

Research paper thumbnail of Detection of viruses by counting single fluorescent genetically biotinylated reporter immunophage using a lateral flow assay

ACS applied materials & interfaces, Jan 4, 2015

We demonstrated a lateral flow immunoassay (LFA) for detection of viruses using fluorescently lab... more We demonstrated a lateral flow immunoassay (LFA) for detection of viruses using fluorescently labeled M13 bacteriophage as reporters and single-reporter counting as the readout. AviTag-biotinylated M13 phage were functionalized with antibodies using avidin-biotin conjugation and fluorescently labeled with AlexaFluor 555. Individual phage bound to target viruses (here MS2 as a model) captured on an LFA membrane strip were imaged using epi-fluorescence microscopy. Using automated image processing, we counted the number of bound phage in micrographs as a function of target concentration. The resultant assay was more sensitive than enzyme-linked immunosorbent assays and traditional colloidal-gold nanoparticle LFAs for direct detection of viruses.

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