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    Tuning the Surface Interactions between Single Cells and an OSTE plus Microwell Array for Enhanced Single Cell Manipulation

    Year: 2021

    Journal: ACS Appl. Mater. Interfaces, Volume 13, JAN 20, page 2316–2326

    Authors: Breukers, Jolien; Horta, Sara; Struyfs, Caroline; Spasic, Dragana; Feys, Hendrik B.; Geukens, Nick; Thevissen, Karin; Cammue, Bruno P. A.; Vanhoorelbeke, Karen; Lammertyn, Jeroen

    Organizations: KU Leuven [IOFm/05/022, C24/16/022, C3/19/024, SARS-CoV-2 mAb-OF2]; European Union [675412]; Research Foundation Flanders [1S38618N, 11A1719N, G042918N, G090120N, G084818N, G080016N, G0C6418N]; IOF, KU Leuven [IOFm/05/022]

    Keywords: single cell manipulation; OSTE; microwell array; optical tweezers; microfluidics; yeast cells; B cells

    Retrieving single cells of interest from an array of microwells for further off-chip analysis is crucial in numerous biological applications. To this end, several single cell manipulation strategies have been developed, including optical tweezers (OT). OT represent a unique approach for contactless cell retrieval, but their performance is often suboptimal due to nonspecific cell adhesion to the microwell surface. In this study, we focused on improving the surface chemistry of microwell arrays to ensure efficient single cell manipulation using OT. For this purpose, the surface of an off-stoichiometry thiol-ene-epoxy (OSTE+) microwell array was grafted with polyethylene glycol (PEG) molecules with different molecular weights: PEG 360, PEG 500, PEG 2000, and a PEG Mix (an equimolar ratio of PEG 500 and PEG 2000). Contact angle measurements showed that the PEG grafting process resulted in an increased surface energy, which was stable for at least 16 weeks. Next, cell adhesion of two cell types, baker's yeast (Saccharomyces cerevisiae) and human B cells, to surfaces treated with different PEGs was evaluated by registering the presence of cellular motion inside microwells and the efficiency of optical lifting of cells that display motion. Optimal results were obtained for surfaces grafted with PEG 2000 and PEG Mix, reaching an average fraction of cells with motion of over 93% and an average lifting efficiency of over 96% for both cell types. Upon the integration of this microwell array with a polydimethylsiloxane (PDMS) microfluidic channel, PEG Mix resulted in proper washing of non-seeded cells. We further demonstrated the wide applicability of the platform by manipulating non-responding yeast cells to antifungal treatment and B cells expressing surface IgG antibodies. The combination of the optimized microwell surface with continuous microfluidics results in a powerful and versatile platform, allowing high-throughput single cell studies and retrieval of target cells for off-chip analysis.
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