A microwell array platform to print and measure biomolecules produced by single cells

Fikri Abali, Joska Johannes Broekmaat, Arjan G.J. Tibbe, R.B.M. Schasfoort, Leonie Laura Zeune, L.W.M.M. Terstappen* (Corresponding Author)

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)
20 Downloads (Pure)

Abstract

Here we describe a combined method to monitor the secretion of molecules produced by single cells, followed by a method to isolate the individual cells that produced these molecules. The method is based on a self-sorting microwell chip that is connected to an activated membrane that collects the produced molecules. The produced molecules are printed by diffusion in small spots onto the membrane. The location of the printed spots can be correlated to the microwell number and the cell that produced these molecules. To demonstrate the method, we used the EpCAM antibody producing hybridoma cell line VU1D9 and a genetically engineered CHO cell-line producing Her2. VU1D9 cells produced 4.6 ± 5.6 pg (mean ± SD) of EpCAM antibody per 24 h and CHO cells 6.5 ± 8.2 pg per 24 h of Herceptin antibody.
Original languageEnglish
Pages (from-to)1850-1859
Number of pages10
JournalLab on a chip
Volume19
Issue number10
DOIs
Publication statusPublished - 21 May 2019

Keywords

  • UT-Hybrid-D
  • Cell isolation
  • Microwell array
  • CHO cells
  • Antibody production
  • Protein secretion dynamics
  • Elispot
  • Fluorospot
  • Single cell expansion
  • Single cell protein secretion

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