4.3 Article

Ultra-low fouling photocrosslinked coatings for the selective capture of cells expressing CD44

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ELSEVIER
DOI: 10.1016/j.msec.2020.111630

Keywords

Coatings; Biofouling; Phage display; Peptide; CD44; Biointerface

Funding

  1. JSPS KAKENHI [18K05249, 18K19907]
  2. NIMS Joint Research Hub Program
  3. CSIRO's Active Integrated Matter Future Science Platform
  4. Australia-Japan Foundation
  5. Grants-in-Aid for Scientific Research [18K05249, 18K19907] Funding Source: KAKEN

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The study demonstrated a novel approach for selectively binding specific cells by incorporating peptide monomers into ultra-low fouling coatings. This method shows potential applications in surface cell binding selectivity and maintains excellent anti-biofouling properties.
The effective control of biointerfacial interactions is of outstanding interest in a broad range of biomedical applications, ranging from cell culture tools to biosensors and implantable medical devices. For many of these applications, highly specific interactions between cells and material surfaces are desired. Sophisticated control over these interactions requires reducing or preventing non-specific interactions on the one hand and displaying highly specific signals that can be recognized by extracellular receptors on the other. We have recently developed ultra-low fouling coatings that can be applied in a single step using photoreactive copolymers of 2-hydroxypropyl acrylamide and N-benzophenone acrylamide. Here, we have expanded this approach by incorporating polymerizable peptide monomers into these copolymers. The monomers QQGWFGAGK(acrylamide) and acrylamide-GAGQQGWF were synthesized after identifying the QQGWF sequence as a binding motif for CD44 by phage display for the first time. Our results demonstrate that UV-crosslinked coatings fabricated using the QQGWFGAGK(acrylamide) monomer are effective at selectively binding hMSC in the presence of HepG2 and HEK293 cells due to the difference in CD44 expression. Our results also demonstrate that the peptide modified coatings retain their low biofouling character using a BCA protein binding assay as well as an E. coli bacterial attachment assay over a 24 h period. Our approach provides an alternative to traditional integrin-mediated selective cell binding on surfaces and opens the door to new diagnostic applications, exploiting the fact that the transmembrane protein CD44 is highly expressed in multiple diseases.

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