Flow cytometric immunoassay using E. coli with autodisplayed Z-domains

• Flow cytometry was used for simultaneous detection of multiple analytes using E. coli cells.
• E. coli cells with and without fluorescence in cytosol were used for multiple analyte detection.
• E. coli cell with autodisplayed Z-domains was used for hyper sensitive immunoassay.
• Flow cytometry based multiple detection was demonstrated with HBsAg and CRP as model analytes.

Recently, we reported a highly sensitive immunoassay using Escherichia coli cells with autodisplayed Z-domains. In this work, E. coli cells with autodisplayed Z-domains were applied to the flow-cytometry-based simultaneous detection of multiple analytes. The E. coli cells were doubly transfected to express a fluorescent protein (tdTomato) in the cytosol and the autodisplayed Z-domains on the outer membrane. By using E. coli cells with only the autodisplayed Z-domains, immunoassay of multiple analytes could be performed simultaneously on the same sample. Flow cytometry can be used to identify the immunoassay type by simultaneously detecting the fluorescence signal from the cytosol (tdTomato) and the fluorescence from the outer membrane, enabling the quantification of bound analytes after treatment with additional fluorescently labeled antibodies. To demonstrate the immunoassay of multiple analytes by using flow cytometry, human hepatitis B virus surface antigen (HBsAg) and C-reactive protein (CRP), a broad spectrum inflammation marker, were used as model analytes.