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1.
Proc Natl Acad Sci U S A ; 107(14): 6264-9, 2010 Apr 06.
Article in English | MEDLINE | ID: mdl-20308580

ABSTRACT

The interaction between cells and nanostructured materials is attracting increasing interest, because of the possibility to open up novel concepts for the design of smart nanobiomaterials with active biological functionalities. In this frame we investigated the response of human neuroblastoma cell line (SH-SY5Y) to gold surfaces with different levels of nanoroughness. To achieve a precise control of the nanoroughness with nanometer resolution, we exploited a wet chemistry approach based on spontaneous galvanic displacement reaction. We demonstrated that neurons sense and actively respond to the surface nanotopography, with a surprising sensitivity to variations of few nanometers. We showed that focal adhesion complexes, which allow cellular sensing, are strongly affected by nanostructured surfaces, leading to a marked decrease in cell adhesion. Moreover, cells adherent on nanorough surfaces exhibit loss of neuron polarity, Golgi apparatus fragmentation, nuclear condensation, and actin cytoskeleton that is not functionally organized. Apoptosis/necrosis assays established that nanoscale features induce cell death by necrosis, with a trend directly related to roughness values. Finally, by seeding SH-SY5Y cells onto micropatterned flat and nanorough gold surfaces, we demonstrated the possibility to realize substrates with cytophilic or cytophobic behavior, simply by fine-tuning their surface topography at nanometer scale. Specific and functional adhesion of cells occurred only onto flat gold stripes, with a clear self-alignment of neurons, delivering a simple and elegant approach for the design and development of biomaterials with precise nanostructure-triggered biological responses.


Subject(s)
Nanostructures/ultrastructure , Neurons/ultrastructure , Cell Adhesion , Cell Line, Tumor , Cell Shape , Humans , Microscopy, Atomic Force , Microscopy, Confocal
2.
Chemphyschem ; 10(9-10): 1471-7, 2009 Jul 13.
Article in English | MEDLINE | ID: mdl-19496082

ABSTRACT

The recombinant production of a novel chimeric polyprotein is described. The new protein contains either wild-type beta(2)-microglobulin (beta(2)m) or its truncated variant (DeltaN6 beta(2)m) (see picture). Structural characterization is achieved by means of single-molecule force spectroscopy studies of specific beta(2)m regions which could be involved in amyloidogenesis.


Subject(s)
beta 2-Microglobulin/chemistry , Amyloidosis , Microscopy, Atomic Force , Protein Engineering , Protein Folding , Recombinant Proteins/chemistry , Spectrometry, Fluorescence
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