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

Eva A. van Aalen, Bas J.H.M. Rosier, Tom Jansen, Simone F.A. Wouters, Robin T. Vermathen, Harmen J. van der Veer, José Yeste Lozano, Sheeza Mughal, Juan M. Fernández-Costa, Javier Ramón-Azcón, Jaap M.J. den Toonder, Maarten Merkx (Corresponding author)

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Samenvatting

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.

Originele taal-2Engels
Pagina's (van-tot)8922-8931
Aantal pagina's10
TijdschriftAnalytical Chemistry
Volume95
Nummer van het tijdschrift23
DOI's
StatusGepubliceerd - 13 jun. 2023

Bibliografische nota

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.

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