Anti-biofouling surface with sub-20 nm heterogeneous nanopatterns

2015 ◽  
Vol 3 (6) ◽  
pp. 1157-1162 ◽  
Author(s):  
Lei Shen ◽  
Jun Xie ◽  
Juan Tao ◽  
Jintao Zhu
Keyword(s):  
Cell Surface ◽  
Molecular Level ◽  
Surface Interactions ◽  
Protein Surface ◽  
Surface Cell ◽  
Cell Surface Interactions ◽  
20 Nm ◽  
Control Protein

We have developed a nanometer-sized heterogeneous pattern with an excellent anti-biofouling property to control protein–surface/cell–surface interactions at the molecular level.

Stimuli-responsive interfaces and systems for the control of protein–surface and cell–surface interactions

Biomaterials ◽  
2009 ◽  
Vol 30 (9) ◽  
pp. 1827-1850 ◽  
Author(s):  
Martin A. Cole ◽  
Nicolas H. Voelcker ◽  
Helmut Thissen ◽  
Hans J. Griesser
Keyword(s):  
Cell Surface ◽  
Surface Interactions ◽  
Stimuli Responsive ◽  
Protein Surface ◽  
Cell Surface Interactions

scholarly journals Automated synthesis of sialylated oligosaccharides

2012 ◽  
Vol 8 ◽  
pp. 1601-1609 ◽  
Author(s):  
Davide Esposito ◽  
Mattan Hurevich ◽  
Bastien Castagner ◽  
Cheng-Chung Wang ◽  
Peter H Seeberger
Keyword(s):  
Sialic Acid ◽  
Cell Surface ◽  
Molecular Level ◽  
Surface Interactions ◽  
Automated Synthesis ◽  
Oligosaccharide Synthesis ◽  
Biological Functions ◽  
Rapid Access ◽  
Cell Surface Interactions ◽  
Automated Platform

Sialic acid-containing glycans play a major role in cell-surface interactions with external partners such as cells and viruses. Straightforward access to sialosides is required in order to study their biological functions on a molecular level. Here, automated oligosaccharide synthesis was used to facilitate the preparation of this class of biomolecules. Our strategy relies on novel sialyl α-(2→3) and α-(2→6) galactosyl imidates, which, used in combination with the automated platform, provided rapid access to a small library of conjugation-ready sialosides of biological relevance.

scholarly journals Endogenous hyaluronate-cell surface interactions in 3T3 and simian virus-transformed 3T3 cells.

1984 ◽  
Vol 259 (15) ◽  
pp. 9440-9446
Author(s):  
R L Goldberg ◽  
J D Seidman ◽  
G Chi-Rosso ◽  
B P Toole
Keyword(s):  
Cell Surface ◽  
Surface Interactions ◽  
Simian Virus ◽  
3T3 Cells ◽  
Cell Surface Interactions

Effects of surface-bound and intravenously administered heparin on cell-surface interactions: inflammation and coagulation

Perfusion ◽  
2013 ◽  
Vol 28 (3) ◽  
pp. 263-271 ◽  
Author(s):  
G Johnson ◽  
B Curry ◽  
L Cahalan ◽  
R Prater ◽  
J Biggerstaff ◽  
...  
Keyword(s):  
Cell Surface ◽  
Surface Interactions ◽  
Cell Surface Interactions

Anti-fouling nano-Ag/SiO2 ormosil treatments for building materials: The role of cell-surface interactions on toxicity and bioreceptivity

2021 ◽  
Vol 153 ◽  
pp. 106120
Author(s):  
Marcia Domínguez ◽  
Rafael Zarzuela ◽  
Ignacio Moreno-Garrido ◽  
María Carbú ◽  
Jesús M. Cantoral ◽  
...  
Keyword(s):  
Cell Surface ◽  
Building Materials ◽  
Surface Interactions ◽  
Cell Surface Interactions

Cell surface interactions in conjugation: Tetrahymena ciliary membrane vesicles

1984 ◽  
Vol 4 (4) ◽  
pp. 681-687
Author(s):  
B Love ◽  
M B Rotheim
Keyword(s):  
Cell Surface ◽  
Mating Type ◽  
Mammalian Cells ◽  
Membrane Vesicles ◽  
Surface Interactions ◽  
Dependent Manner ◽  
Concentration Dependent Manner ◽  
Ciliary Membrane ◽  
Adhesion Sites ◽  
Cell Surface Interactions

Tetrahymena ciliary membrane vesicles are shown to interact with preconjugant cells in a mating type-specific way. When cells are treated with vesicles of a different mating type before mixing for conjugation, cell pairing is enhanced, and the normal prepairing period is partially eliminated. This enhancement is mating type specific since it is not observed after pretreatment of cells with vesicles of their own mating type. In contrast, when vesicles are added at the time of mixing of two starved cultures, cell pairing is delayed in a concentration-dependent manner. By varying the conditions, we demonstrated enhancement or inhibition, or both. These results are interpreted in terms of two independent interactions of cells with vesicles. We suggest that first, vesicles substitute for another cell in cell-cell prepairing interaction and second, vesicles compete for adhesion sites produced during the prepairing period. Finally, the data presented are summarized within a speculative framework that calls attention to potential analogies with hormone-receptor signaling in mammalian cells.

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