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Integrated Bioluminescent Immunoassays for High-Throughput Sampling and Continuous Monitoring of Cytokines

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Abstract

Immunoassays show great potential for the detection of low levels of cytokines, due to their high sensitivity and excellent specificity. There is a particular demand for biosensors that enable both high-throughput screening and continuous monitoring of clinically relevant cytokines such as interleukin-6 (IL-6) and tumor necrosis factor-α (TNFα). To this end, we here introduce a novel bioluminescent immunoassay based on the ratiometric plug-and-play immunodiagnostics (RAPPID) platform, with an improved intrinsic signal-to-background and an >80-fold increase in the luminescent signal. The new dRAPPID assay, comprising a dimeric protein G adapter connected via a semiflexible linker, was applied to detect the secretion of IL-6 by breast carcinoma cells upon TNFα stimulation and the production of low concentrations of IL-6 (∼18 pM) in an endotoxin-stimulated human 3D muscle tissue model. Moreover, we integrated the dRAPPID assay in a newly developed microfluidic device for the simultaneous and continuous monitoring of changes in IL-6 and TNFα in the low-nanomolar range. The luminescence-based read-out and the homogeneous nature of the dRAPPID platform allowed for detection with a simple measurement setup, consisting of a digital camera and a light-sealed box. This permits the usage of the continuous dRAPPID monitoring chip at the point of need, without the requirement for complex or expensive detection techniques.

Original languageEnglish
Pages (from-to)8922-8931
Number of pages10
JournalAnalytical Chemistry
Volume95
Issue number23
DOIs
Publication statusPublished - 13 Jun 2023

Bibliographical note

Funding Information:
We thank M. Jouy Bar and P. Zuo for their helpful discussions and providing the MDA MB 231 cells and G. E. López-Muñoz for helping with the initial microfluidic experiments. E. Hanckmann and Y. Ni are thanked for their contributions in cloning the protein G adapter dimers and E. Moonen is thanked for the helpful discussions and support in the lab. This work was supported by RAAK.PRO Printing makes sense (RAAK.PRO02.066) and by an ICMS-IBEC collaboration grant.

Funding

We thank M. Jouy Bar and P. Zuo for their helpful discussions and providing the MDA MB 231 cells and G. E. López-Muñoz for helping with the initial microfluidic experiments. E. Hanckmann and Y. Ni are thanked for their contributions in cloning the protein G adapter dimers and E. Moonen is thanked for the helpful discussions and support in the lab. This work was supported by RAAK.PRO Printing makes sense (RAAK.PRO02.066) and by an ICMS-IBEC collaboration grant.

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