TY - JOUR
T1 - Cell-based surface plasmon resonance approach for monitoring the inhibitory effect of Evasin-3 on Interleukin-8
AU - Zhao, Yuandi
AU - Hadavi, Darya
AU - Scurti, Elena
AU - Viitala, Tapani
AU - Dijkgraaf, Ingrid
AU - Honing, Maarten
N1 - Funding Information:
We would like to thank Anjusha Mathew (Maastricht University) for the help of MS measurement. T.V and E.S would like to acknowledge funding from the Finnish Research Impact Foundation and the Doctoral Programme in Drug Research. For this project, D.H acknowledges the financial support from the project DARTBAC (with project number NWA.1292.19.354) of the research programme NWA-ORC which is (partly) financed by the Dutch Research Council (NWO).
Publisher Copyright:
© 2025 The Authors
PY - 2025/7/15
Y1 - 2025/7/15
N2 - Surface plasmon resonance (SPR) is a widely utilized technique for measuring the kinetics of molecular interactions. However, in dynamic living systems, the kinetics of target-ligand interactions may differ. Additionally, most cellular assays rely on end-point measurements, lacking the ability to monitor cellular interactions in real-time. In this study, a real-time cell-based SPR method was developed to investigate the inhibitory effect of small protein evasin-3 on the interaction between G protein-coupled receptors (GPCRs) and chemokine interleukin-8 (CXCL8). The interaction between CXCL8 and evasin-3 was first measured via a traditional SPR kinetic study. Their interaction was then confirmed and characterized using mass spectrometry, providing detailed insights into the complex formation of these two proteins. Endothelial EA.hy926 cells were immobilized on the SPR gold sensor, and real-time SPR response signals were monitored during stimulation with CXCL8, evasin-3 and their mixture. The results demonstrated the inhibitory effect of evasin-3 on the interaction between CXCL8 and GPCRs on EA.hy926 cells. This cell-based SPR method provides a valuable, physiologically relevant approach for studying inhibitory effects in living cells, presenting an effective alternative for analyzing complex molecular interactions.
AB - Surface plasmon resonance (SPR) is a widely utilized technique for measuring the kinetics of molecular interactions. However, in dynamic living systems, the kinetics of target-ligand interactions may differ. Additionally, most cellular assays rely on end-point measurements, lacking the ability to monitor cellular interactions in real-time. In this study, a real-time cell-based SPR method was developed to investigate the inhibitory effect of small protein evasin-3 on the interaction between G protein-coupled receptors (GPCRs) and chemokine interleukin-8 (CXCL8). The interaction between CXCL8 and evasin-3 was first measured via a traditional SPR kinetic study. Their interaction was then confirmed and characterized using mass spectrometry, providing detailed insights into the complex formation of these two proteins. Endothelial EA.hy926 cells were immobilized on the SPR gold sensor, and real-time SPR response signals were monitored during stimulation with CXCL8, evasin-3 and their mixture. The results demonstrated the inhibitory effect of evasin-3 on the interaction between CXCL8 and GPCRs on EA.hy926 cells. This cell-based SPR method provides a valuable, physiologically relevant approach for studying inhibitory effects in living cells, presenting an effective alternative for analyzing complex molecular interactions.
KW - Cellular assay
KW - Evasin-3
KW - G protein-coupled receptors
KW - Interleukin-8
KW - Surface plasmon resonance
KW - Target-ligand interaction
U2 - 10.1016/j.aca.2025.344091
DO - 10.1016/j.aca.2025.344091
M3 - Article
SN - 0003-2670
VL - 1359
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
M1 - 344091
ER -