Related Experiment Video
Updated: Mar 27, 2026

A Label-free Technique for the Spatio-temporal Imaging of Single Cell Secretions
Published on: November 23, 2015
Cancer-Cells on Chip for Label-Free Detection of Secreted Molecules
Ophélie I Berthuy1, Loïc J Blum2, Christophe A Marquette3
1Laboratoire de Génie Enzymatique, Membranes Biomimétiques et Assemblages Supramoléculaires-Institut de Chimie et Biochimie Moléculaires et Supramoléculaires-Université Claude Bernard Lyon 1, Villeurbanne 69100, France. berthuy@scienion.de.
Abstract:
In the present report, we are making the proof of concept of cell small populations (from 1 to 100 cells) spotting, culture and secretion detection on a gold surface. In order to keep the cells in a hydrated environment during the robotized micropipetting and to address different cell lines on a single chip, a biocompatible alginate polymer was used. This approach enables the encapsulation of the cell in a very small volume (30 nL), directly on the substrate and permits a precise control of the number of cells in each alginate bead. After 24 h of culture, the adherent cells are ready for surface plasmon resonance imaging (SPRi) experimentation. To enable the detection of secreted proteins, various antibodies are immobilized in an organized manner on a SPRi sensor and permitted the multiplex detection of different proteins secreted by the different cultured cell lines. Evidence of the real-time detection will be presented for Prostate Specific Antigen (PSA) and β-2-microglobulin (B2M) secreted by prostate cancer cells following induction by dihydrotestosterone (DHT). Different kinetics for the two secreted proteins were then demonstrated and precisely determined using the chip.

