| Literature DB >> 32764330 |
Ivana Víšová1, Barbora Smolková1, Mariia Uzhytchak1, Markéta Vrabcová1, Djamel Eddine Chafai1, Milan Houska1, Matěj Pastucha2, Petr Skládal2, Zdeněk Farka2, Alexandr Dejneka1, Hana Vaisocherová-Lísalová1.
Abstract
Cells are continuously sensing their microenvironment and subsequently respond to different physicochemical cues by the activation or inhibition of different signaling pathways. To study a very complex cellular response, it is necessary to diminish background environmental influences and highlight the particular event. However, surface-driven nonspecific interactions of the abundant biomolecules from the environment influence the targeted cell response significantly. Yes-associated protein (YAP) translocation may serve as a marker of human hepatocellular carcinoma (Huh7) cell responses to the extracellular matrix and surface-mediated stresses. Here, we propose a platform of tunable functionable antifouling poly(carboxybetain) (pCB)-based brushes to achieve a molecularly clean background for studying arginine, glycine, and aspartic acid (RGD)-induced YAP-connected mechanotransduction. Using two different sets of RGD-functionalized zwitterionic antifouling coatings with varying compositions of the antifouling layer, a clear correlation of YAP distribution with RGD functionalization concentrations was observed. On the other hand, commonly used surface passivation by the oligo(ethylene glycol)-based self-assembled monolayer (SAM) shows no potential to induce dependency of the YAP distribution on RGD concentrations. The results indicate that the antifouling background is a crucial component of surface-based cellular response studies, and pCB-based zwitterionic antifouling brush architectures may serve as a potential next-generation easily functionable surface platform for the monitoring and quantification of cellular processes.Entities:
Keywords: antifouling polymer brushes; cell mechanotransduction; cell signaling; functional biointerfaces; surface modification; zwitterionic material
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Year: 2020 PMID: 32764330 PMCID: PMC7464033 DOI: 10.3390/biom10081146
Source DB: PubMed Journal: Biomolecules ISSN: 2218-273X