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Patterned and switchable surfaces for biomaterial applications

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Chapter 4 – Formation of a chemically patterned substrate <strong>for</strong> cell microarray <strong>applications</strong>However, the key advantage of this approach is the integration of the celladhesion regulating pattern with the subsequent <strong>for</strong>mation of a small-molecule,protein, DNA or RNA microarray. By way of a demonstration, a TCM was preparedby first spotting an array of DNA vectors using pEGFP-N1, a plasmid encoding <strong>for</strong> aGFP, <strong>and</strong> pDsRed2, a plasmid encoding <strong>for</strong> a RFP, along with Effectene transfectionagent on top of the already prepared PLLc polymer array. Since surface patterning<strong>and</strong> microarray <strong>for</strong>mation are carried out on the same instrument, alignment of thetwo surface patterns was easily achieved. At neutral pH, PLL is positively charged,thus stabilising electrostatically the deposited DNA. The interactions between DNA<strong>and</strong> PAA, polyallylamine (PALA), PEI, PLL <strong>and</strong> PVP surface coatings was assessedby atomic <strong>for</strong>ce microscopy <strong>for</strong>ce measurements (Appendix 2). This demonstratedthe electrostatic nature of interactions between DNA <strong>and</strong> PALA, PEI <strong>and</strong> PLL. ThePEG surface has previously been shown to restrict DNA adsorption, hencepreventing surface diffusion of the DNA spots on the surface [188, 207]. HEK-293cells were subsequently seeded onto the array <strong>and</strong> were visualised by fluorescencemicroscopy after 48 hr incubation at 37 °C to check <strong>for</strong> reverse transfection. Acheckerboard pattern of red <strong>and</strong> green cells resulted (Figure 4.7A), whereupon cellsfluorescing green were localised to regions where pEGFP-N1 had been spotted onPLLc (Figure 4.7B) whilst cells fluorescing red were localised to regions wherepDsRed2 had been deposited on PLLc (Figure 4.7C), confirming that reversetransfection had occurred. There were no fluorescent cells found outside the PLLcregions. Furthermore, green <strong>and</strong> red fluorescing cells were not observed on the samespot, demonstrating the absence of cross-contamination. Typically, transfectionefficiencies of 15-20% were observed, which is similar to previously reportedefficiencies [29, 35].4-150

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