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Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures

The understanding of phenomena involved in the self-assembling of bio-inspired biomaterials acting as three-dimensional scaffolds for regenerative medicine applications is a necessary step to develop effective therapies in neural tissue engineering. We investigated the self-assembled nanostructures...

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Autores principales: Taraballi, Francesca, Natalello, Antonino, Campione, Marcello, Villa, Omar, Doglia, Silvia M., Paleari, Alberto, Gelain, Fabrizio
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821182/
https://www.ncbi.nlm.nih.gov/pubmed/20162033
http://dx.doi.org/10.3389/neuro.16.001.2010
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author Taraballi, Francesca
Natalello, Antonino
Campione, Marcello
Villa, Omar
Doglia, Silvia M.
Paleari, Alberto
Gelain, Fabrizio
author_facet Taraballi, Francesca
Natalello, Antonino
Campione, Marcello
Villa, Omar
Doglia, Silvia M.
Paleari, Alberto
Gelain, Fabrizio
author_sort Taraballi, Francesca
collection PubMed
description The understanding of phenomena involved in the self-assembling of bio-inspired biomaterials acting as three-dimensional scaffolds for regenerative medicine applications is a necessary step to develop effective therapies in neural tissue engineering. We investigated the self-assembled nanostructures of functionalized peptides featuring four, two or no glycine-spacers between the self-assembly sequence RADA16-I and the functional biological motif PFSSTKT. The effectiveness of their biological functionalization was assessed via in vitro experiments with neural stem cells (NSCs) and their molecular assembly was elucidated via atomic force microscopy, Raman and Fourier Transform Infrared spectroscopy. We demonstrated that glycine-spacers play a crucial role in the scaffold stability and in the exposure of the functional motifs. In particular, a glycine-spacer of four residues leads to a more stable nanostructure and to an improved exposure of the functional motif. Accordingly, the longer spacer of glycines, the more effective is the functional motif in both eliciting NSCs adhesion, improving their viability and increasing their differentiation. Therefore, optimized designing strategies of functionalized biomaterials may open, in the near future, new therapies in tissue engineering and regenerative medicine.
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spelling pubmed-28211822010-02-16 Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures Taraballi, Francesca Natalello, Antonino Campione, Marcello Villa, Omar Doglia, Silvia M. Paleari, Alberto Gelain, Fabrizio Front Neuroengineering Neuroscience The understanding of phenomena involved in the self-assembling of bio-inspired biomaterials acting as three-dimensional scaffolds for regenerative medicine applications is a necessary step to develop effective therapies in neural tissue engineering. We investigated the self-assembled nanostructures of functionalized peptides featuring four, two or no glycine-spacers between the self-assembly sequence RADA16-I and the functional biological motif PFSSTKT. The effectiveness of their biological functionalization was assessed via in vitro experiments with neural stem cells (NSCs) and their molecular assembly was elucidated via atomic force microscopy, Raman and Fourier Transform Infrared spectroscopy. We demonstrated that glycine-spacers play a crucial role in the scaffold stability and in the exposure of the functional motifs. In particular, a glycine-spacer of four residues leads to a more stable nanostructure and to an improved exposure of the functional motif. Accordingly, the longer spacer of glycines, the more effective is the functional motif in both eliciting NSCs adhesion, improving their viability and increasing their differentiation. Therefore, optimized designing strategies of functionalized biomaterials may open, in the near future, new therapies in tissue engineering and regenerative medicine. Frontiers Research Foundation 2010-02-08 /pmc/articles/PMC2821182/ /pubmed/20162033 http://dx.doi.org/10.3389/neuro.16.001.2010 Text en Copyright © 2010 Taraballi, Natalello, Campione, Villa, Doglia, Paleari and Gelain. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Taraballi, Francesca
Natalello, Antonino
Campione, Marcello
Villa, Omar
Doglia, Silvia M.
Paleari, Alberto
Gelain, Fabrizio
Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures
title Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures
title_full Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures
title_fullStr Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures
title_full_unstemmed Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures
title_short Glycine-Spacers Influence Functional Motifs Exposure and Self-Assembling Propensity of Functionalized Substrates Tailored for Neural Stem Cell Cultures
title_sort glycine-spacers influence functional motifs exposure and self-assembling propensity of functionalized substrates tailored for neural stem cell cultures
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821182/
https://www.ncbi.nlm.nih.gov/pubmed/20162033
http://dx.doi.org/10.3389/neuro.16.001.2010
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