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Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies

Water soluble fibers of PEGylated tetra-phenylalanine (F4), chemically modified at the N-terminus with the DOTA chelating agent, have been proposed as innovative contrast agent (CA) in Magnetic Resonance Imaging (MRI) upon complexation of the gadolinium ion. An in-depth structural characterization o...

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Autores principales: Diaferia, Carlo, Mercurio, Flavia Anna, Giannini, Cinzia, Sibillano, Teresa, Morelli, Giancarlo, Leone, Marilisa, Accardo, Antonella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879547/
https://www.ncbi.nlm.nih.gov/pubmed/27220817
http://dx.doi.org/10.1038/srep26638
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author Diaferia, Carlo
Mercurio, Flavia Anna
Giannini, Cinzia
Sibillano, Teresa
Morelli, Giancarlo
Leone, Marilisa
Accardo, Antonella
author_facet Diaferia, Carlo
Mercurio, Flavia Anna
Giannini, Cinzia
Sibillano, Teresa
Morelli, Giancarlo
Leone, Marilisa
Accardo, Antonella
author_sort Diaferia, Carlo
collection PubMed
description Water soluble fibers of PEGylated tetra-phenylalanine (F4), chemically modified at the N-terminus with the DOTA chelating agent, have been proposed as innovative contrast agent (CA) in Magnetic Resonance Imaging (MRI) upon complexation of the gadolinium ion. An in-depth structural characterization of PEGylated F4-fibers, in presence (DOTA-L(6)-F4) and in absence of DOTA (L(6)-F4), is reported in solution and at the solid state, by a multiplicity of techniques including CD, FTIR, NMR, DLS, WAXS and SAXS. This study aims to better understand how the aggregation process influences the performance of nanostructures as MRI CAs. Critical aggregation concentrations for L(6)-F4 (43 μM) and DOTA-L(6)-F4 (75 μM) indicate that self-aggregation process occurs in the same concentration range, independently of the presence of the CA. The driving force for the aggregation is the π-stacking between the side chains of the aromatic framework. CD, FTIR and WAXS measurements indicate an antiparallel β-sheet organization of the monomers in the resulting fibers. Moreover, WAXS and FTIR experiments point out that in solution the nanomaterials retain the same morphology and monomer organizations of the solid state, although the addition of the DOTA chelating agent affects the size and the degree of order of the fibers.
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spelling pubmed-48795472016-06-07 Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies Diaferia, Carlo Mercurio, Flavia Anna Giannini, Cinzia Sibillano, Teresa Morelli, Giancarlo Leone, Marilisa Accardo, Antonella Sci Rep Article Water soluble fibers of PEGylated tetra-phenylalanine (F4), chemically modified at the N-terminus with the DOTA chelating agent, have been proposed as innovative contrast agent (CA) in Magnetic Resonance Imaging (MRI) upon complexation of the gadolinium ion. An in-depth structural characterization of PEGylated F4-fibers, in presence (DOTA-L(6)-F4) and in absence of DOTA (L(6)-F4), is reported in solution and at the solid state, by a multiplicity of techniques including CD, FTIR, NMR, DLS, WAXS and SAXS. This study aims to better understand how the aggregation process influences the performance of nanostructures as MRI CAs. Critical aggregation concentrations for L(6)-F4 (43 μM) and DOTA-L(6)-F4 (75 μM) indicate that self-aggregation process occurs in the same concentration range, independently of the presence of the CA. The driving force for the aggregation is the π-stacking between the side chains of the aromatic framework. CD, FTIR and WAXS measurements indicate an antiparallel β-sheet organization of the monomers in the resulting fibers. Moreover, WAXS and FTIR experiments point out that in solution the nanomaterials retain the same morphology and monomer organizations of the solid state, although the addition of the DOTA chelating agent affects the size and the degree of order of the fibers. Nature Publishing Group 2016-05-25 /pmc/articles/PMC4879547/ /pubmed/27220817 http://dx.doi.org/10.1038/srep26638 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Diaferia, Carlo
Mercurio, Flavia Anna
Giannini, Cinzia
Sibillano, Teresa
Morelli, Giancarlo
Leone, Marilisa
Accardo, Antonella
Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
title Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
title_full Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
title_fullStr Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
title_full_unstemmed Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
title_short Self-assembly of PEGylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
title_sort self-assembly of pegylated tetra-phenylalanine derivatives: structural insights from solution and solid state studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879547/
https://www.ncbi.nlm.nih.gov/pubmed/27220817
http://dx.doi.org/10.1038/srep26638
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