摘要
Multiplexed analysis of molecules with different concentrations requires assays with a tunable detection range. A strategy is outlined that uses click chemistry to assemble horseradish peroxidase in a controlled fashion to generate enzyme assemblies as probes for multiplexed bioassays. This controllable assembly of enzymes on detection antibodies allows for lab‐on‐a‐chip immunoassays with a tunable detection range from pg mL\u003csup\u003e?1\u003c/sup\u003e to μg mL\u003csup\u003e?1\u003c/sup\u003e. Simultaneous, multiplexed bioassays of clinically relevant inflammatory biomarkers in serum are demonstrated in one lab‐on‐a‐chip format, with a limit of detection of 0.47 pg mL\u003csup\u003e?1\u003c/sup\u003e for interleukin‐6, 2.6 pg mL\u003csup\u003e?1\u003c/sup\u003e for procalcitonin, and 40 ng mL\u003csup\u003e?1\u003c/sup\u003e for C‐reactive protein. This controlled assembly technique provides a multiplexed platform for simultaneous and quantitative analyses of both low‐abundance and high‐abundance biomarkers with a broad detection range, which holds great promise as a point‐of‐care platform for biomedical diagnostics.
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