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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4879547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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