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The self-assembly of l-histidine might be the cause of histidinemia
l-Histidine is an essential amino acid with unique biochemical and physiological properties. Histidinemia is a disease condition caused by the elevated level of l-histidine in our blood. Mutations in the histidase, an enzyme for the breakdown of histidine, is the cause of the rise in histidine conce...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576791/ https://www.ncbi.nlm.nih.gov/pubmed/37838762 http://dx.doi.org/10.1038/s41598-023-44749-5 |
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author | Ajikumar, Ajitha Premkumar, Anakha Kandara Nikarthil Narayanan, Sunilkumar Puthenpurackal |
author_facet | Ajikumar, Ajitha Premkumar, Anakha Kandara Nikarthil Narayanan, Sunilkumar Puthenpurackal |
author_sort | Ajikumar, Ajitha |
collection | PubMed |
description | l-Histidine is an essential amino acid with unique biochemical and physiological properties. Histidinemia is a disease condition caused by the elevated level of l-histidine in our blood. Mutations in the histidase, an enzyme for the breakdown of histidine, is the cause of the rise in histidine concentration. To our knowledge, no research has been done on why a high concentration of histidine causes histidinemia. In this study, we provide a potential explanation why the elevated levels of histidine in the human body causes histidinemia. In this study we have found that l-histidine self-assembled in water to form nano sheet structures at physiological pH and temperature, using 1D (1)H NMR spectroscopy, diffusion ordered spectroscopy (DOSY) and scanning electron microscope (SEM) techniques. The kinetics of self-assembly has been studied using real time NMR spectroscopy. We observed that both the aromatic ring and aliphatic part are equally contributing to the self-assembly of l-histidine. The symptoms of histidinemia, neurological deficits and speech delays, are similar to that of the neurodegenerative diseases caused by the self-assembly of peptides and proteins. We speculate that the self-assembly of l-histidine might be the cause of histidinemia. |
format | Online Article Text |
id | pubmed-10576791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105767912023-10-16 The self-assembly of l-histidine might be the cause of histidinemia Ajikumar, Ajitha Premkumar, Anakha Kandara Nikarthil Narayanan, Sunilkumar Puthenpurackal Sci Rep Article l-Histidine is an essential amino acid with unique biochemical and physiological properties. Histidinemia is a disease condition caused by the elevated level of l-histidine in our blood. Mutations in the histidase, an enzyme for the breakdown of histidine, is the cause of the rise in histidine concentration. To our knowledge, no research has been done on why a high concentration of histidine causes histidinemia. In this study, we provide a potential explanation why the elevated levels of histidine in the human body causes histidinemia. In this study we have found that l-histidine self-assembled in water to form nano sheet structures at physiological pH and temperature, using 1D (1)H NMR spectroscopy, diffusion ordered spectroscopy (DOSY) and scanning electron microscope (SEM) techniques. The kinetics of self-assembly has been studied using real time NMR spectroscopy. We observed that both the aromatic ring and aliphatic part are equally contributing to the self-assembly of l-histidine. The symptoms of histidinemia, neurological deficits and speech delays, are similar to that of the neurodegenerative diseases caused by the self-assembly of peptides and proteins. We speculate that the self-assembly of l-histidine might be the cause of histidinemia. Nature Publishing Group UK 2023-10-14 /pmc/articles/PMC10576791/ /pubmed/37838762 http://dx.doi.org/10.1038/s41598-023-44749-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ajikumar, Ajitha Premkumar, Anakha Kandara Nikarthil Narayanan, Sunilkumar Puthenpurackal The self-assembly of l-histidine might be the cause of histidinemia |
title | The self-assembly of l-histidine might be the cause of histidinemia |
title_full | The self-assembly of l-histidine might be the cause of histidinemia |
title_fullStr | The self-assembly of l-histidine might be the cause of histidinemia |
title_full_unstemmed | The self-assembly of l-histidine might be the cause of histidinemia |
title_short | The self-assembly of l-histidine might be the cause of histidinemia |
title_sort | self-assembly of l-histidine might be the cause of histidinemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576791/ https://www.ncbi.nlm.nih.gov/pubmed/37838762 http://dx.doi.org/10.1038/s41598-023-44749-5 |
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