Functionalizable Antifouling Coatings as Tunable Platforms for the Stress-Driven Manipulation of Living Cell Machinery.


Journal

Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414

Informations de publication

Date de publication:
05 08 2020
Historique:
received: 20 05 2020
revised: 24 07 2020
accepted: 30 07 2020
entrez: 9 8 2020
pubmed: 9 8 2020
medline: 18 2 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32764330
pii: biom10081146
doi: 10.3390/biom10081146
pmc: PMC7464033
pii:
doi:

Substances chimiques

Acrylamides 0
Coated Materials, Biocompatible 0
Oligopeptides 0
zwitterion carboxybetaine acrylamide 0
arginyl-glycyl-aspartic acid 78VO7F77PN
Proto-Oncogene Proteins c-yes EC 2.7.10.2
YES1 protein, human EC 2.7.10.2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Akademie Věd České Republiky
ID : LQ100101902
Pays : International
Organisme : Ministerstvo Školství, Mládeže a Tělovýchovy
ID : CZ.02.1.01/0.0/0.0/16_019/0000760
Pays : International

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Auteurs

Ivana Víšová (I)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Barbora Smolková (B)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Mariia Uzhytchak (M)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Markéta Vrabcová (M)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Djamel Eddine Chafai (DE)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Milan Houska (M)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Matěj Pastucha (M)

Department of Biochemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic.

Petr Skládal (P)

Department of Biochemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic.

Zdeněk Farka (Z)

Department of Biochemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic.

Alexandr Dejneka (A)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

Hana Vaisocherová-Lísalová (H)

Institute of Physics CAS, Na Slovance 1999/2, 182 21 Prague, Czech Republic.

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Classifications MeSH