4.8 Article

Controllable Assembly of Enzymes for Multiplexed Lab-on-a-Chip Bioassays with a Tunable Detection Range

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 57, 期 25, 页码 7503-7507

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201801815

关键词

Click Chemistry; enzyme assembly; lab-on-a-chip immunoassays; tunable detection range

资金

  1. National Science Foundation of China [81671784, 21505027, 81361140345, 21535001, 81730051, 21761142006]
  2. Ministry of Science and Technology of China [2013YQ190467]
  3. Beijing Nova Program [Z181100006218017]
  4. Chinese Academy of Sciences [2018047, XDA09030305, 121D11KYSB20170026]

向作者/读者索取更多资源

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 pgmL(-1) to gmL(-1). 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 0.47pgmL(-1) for interleukin-6, 2.6 pgmL(-1) for procalcitonin, and 40ngmL(-1) 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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