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Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different?
New peptide dendrimer with Lys-2Arg repeating units was recently studied experimentally by NMR (RSC Advances, 2019, 9, 18018) and tested as gene carrier successfully (Int. J. Mol. Sci., 2020, 21, 3138). The unusual slowing down of the orientational mobility of 2Arg spacers in this dendrimer was reve...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766995/ https://www.ncbi.nlm.nih.gov/pubmed/33371242 http://dx.doi.org/10.3390/ijms21249749 |
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author | Bezrodnyi, Valeriy V. Shavykin, Oleg V. Mikhtaniuk, Sofia E. Neelov, Igor M. Sheveleva, Nadezhda N. Markelov, Denis A. |
author_facet | Bezrodnyi, Valeriy V. Shavykin, Oleg V. Mikhtaniuk, Sofia E. Neelov, Igor M. Sheveleva, Nadezhda N. Markelov, Denis A. |
author_sort | Bezrodnyi, Valeriy V. |
collection | PubMed |
description | New peptide dendrimer with Lys-2Arg repeating units was recently studied experimentally by NMR (RSC Advances, 2019, 9, 18018) and tested as gene carrier successfully (Int. J. Mol. Sci., 2020, 21, 3138). The unusual slowing down of the orientational mobility of 2Arg spacers in this dendrimer was revealed. It has been suggested that this unexpected behavior is caused by the Arg-Arg pairing effect in water, which leads to entanglements between dendrimer branches. In this paper, we determine the reason for this slowing down using atomistic molecular dynamics simulation of this dendrimer. We present that the structural properties of Lys-2Arg dendrimer are close to those of the Lys-2Lys dendrimer at all temperatures (Polymers, 2020, 12, 1657). However, the orientational mobility of the H-H vector in CH [Formula: see text]-N groups of 2Arg spacers in Lys-2Arg dendrimer is significantly slower than the mobility of the same vector in the Lys-2Lys dendrimer. This result is in agreement with the recent NMR experiments for the same systems. We revealed that this difference is not due to the arginine-arginine pairing, but is due to the semiflexibility effect associated with the different contour length from CH [Formula: see text]-N group to the end of the side arginine or lysine segment in spacers. |
format | Online Article Text |
id | pubmed-7766995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77669952020-12-28 Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? Bezrodnyi, Valeriy V. Shavykin, Oleg V. Mikhtaniuk, Sofia E. Neelov, Igor M. Sheveleva, Nadezhda N. Markelov, Denis A. Int J Mol Sci Article New peptide dendrimer with Lys-2Arg repeating units was recently studied experimentally by NMR (RSC Advances, 2019, 9, 18018) and tested as gene carrier successfully (Int. J. Mol. Sci., 2020, 21, 3138). The unusual slowing down of the orientational mobility of 2Arg spacers in this dendrimer was revealed. It has been suggested that this unexpected behavior is caused by the Arg-Arg pairing effect in water, which leads to entanglements between dendrimer branches. In this paper, we determine the reason for this slowing down using atomistic molecular dynamics simulation of this dendrimer. We present that the structural properties of Lys-2Arg dendrimer are close to those of the Lys-2Lys dendrimer at all temperatures (Polymers, 2020, 12, 1657). However, the orientational mobility of the H-H vector in CH [Formula: see text]-N groups of 2Arg spacers in Lys-2Arg dendrimer is significantly slower than the mobility of the same vector in the Lys-2Lys dendrimer. This result is in agreement with the recent NMR experiments for the same systems. We revealed that this difference is not due to the arginine-arginine pairing, but is due to the semiflexibility effect associated with the different contour length from CH [Formula: see text]-N group to the end of the side arginine or lysine segment in spacers. MDPI 2020-12-21 /pmc/articles/PMC7766995/ /pubmed/33371242 http://dx.doi.org/10.3390/ijms21249749 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bezrodnyi, Valeriy V. Shavykin, Oleg V. Mikhtaniuk, Sofia E. Neelov, Igor M. Sheveleva, Nadezhda N. Markelov, Denis A. Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? |
title | Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? |
title_full | Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? |
title_fullStr | Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? |
title_full_unstemmed | Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? |
title_short | Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different? |
title_sort | why the orientational mobility in arginine and lysine spacers of peptide dendrimers designed for gene delivery is different? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766995/ https://www.ncbi.nlm.nih.gov/pubmed/33371242 http://dx.doi.org/10.3390/ijms21249749 |
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