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1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor
BACKGROUND: The 1α,25-dihydroxy-3-epi-vitamin-D(3) (1α,25(OH)(2)-3-epi-D(3)), a natural metabolite of the seco-steroid vitamin D(3), exerts its biological activity through binding to its cognate vitamin D nuclear receptor (VDR), a ligand dependent transcription regulator. In vivo action of 1α,25(OH)...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069065/ https://www.ncbi.nlm.nih.gov/pubmed/21483824 http://dx.doi.org/10.1371/journal.pone.0018124 |
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author | Molnár, Ferdinand Sigüeiro, Rita Sato, Yoshiteru Araujo, Clarisse Schuster, Inge Antony, Pierre Peluso, Jean Muller, Christian Mouriño, Antonio Moras, Dino Rochel, Natacha |
author_facet | Molnár, Ferdinand Sigüeiro, Rita Sato, Yoshiteru Araujo, Clarisse Schuster, Inge Antony, Pierre Peluso, Jean Muller, Christian Mouriño, Antonio Moras, Dino Rochel, Natacha |
author_sort | Molnár, Ferdinand |
collection | PubMed |
description | BACKGROUND: The 1α,25-dihydroxy-3-epi-vitamin-D(3) (1α,25(OH)(2)-3-epi-D(3)), a natural metabolite of the seco-steroid vitamin D(3), exerts its biological activity through binding to its cognate vitamin D nuclear receptor (VDR), a ligand dependent transcription regulator. In vivo action of 1α,25(OH)(2)-3-epi-D(3) is tissue-specific and exhibits lowest calcemic effect compared to that induced by 1α,25(OH)(2)D(3). To further unveil the structural mechanism and structure-activity relationships of 1α,25(OH)(2)-3-epi-D(3) and its receptor complex, we characterized some of its in vitro biological properties and solved its crystal structure complexed with human VDR ligand-binding domain (LBD). METHODOLOGY/PRINCIPAL FINDINGS: In the present study, we report the more effective synthesis with fewer steps that provides higher yield of the 3-epimer of the 1α,25(OH)(2)D(3). We solved the crystal structure of its complex with the human VDR-LBD and found that this natural metabolite displays specific adaptation of the ligand-binding pocket, as the 3-epimer maintains the number of hydrogen bonds by an alternative water-mediated interaction to compensate the abolished interaction with Ser278. In addition, the biological activity of the 1α,25(OH)(2)-3-epi-D(3) in primary human keratinocytes and biochemical properties are comparable to 1α,25(OH)(2)D(3). CONCLUSIONS/SIGNIFICANCE: The physiological role of this pathway as the specific biological action of the 3-epimer remains unclear. However, its high metabolic stability together with its significant biologic activity makes this natural metabolite an interesting ligand for clinical applications. Our new findings contribute to a better understanding at molecular level how natural metabolites of 1α,25(OH)(2)D(3) lead to significant activity in biological systems and we conclude that the C3-epimerization pathway produces an active metabolite with similar biochemical and biological properties to those of the 1α,25(OH)(2)D(3). |
format | Text |
id | pubmed-3069065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30690652011-04-11 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor Molnár, Ferdinand Sigüeiro, Rita Sato, Yoshiteru Araujo, Clarisse Schuster, Inge Antony, Pierre Peluso, Jean Muller, Christian Mouriño, Antonio Moras, Dino Rochel, Natacha PLoS One Research Article BACKGROUND: The 1α,25-dihydroxy-3-epi-vitamin-D(3) (1α,25(OH)(2)-3-epi-D(3)), a natural metabolite of the seco-steroid vitamin D(3), exerts its biological activity through binding to its cognate vitamin D nuclear receptor (VDR), a ligand dependent transcription regulator. In vivo action of 1α,25(OH)(2)-3-epi-D(3) is tissue-specific and exhibits lowest calcemic effect compared to that induced by 1α,25(OH)(2)D(3). To further unveil the structural mechanism and structure-activity relationships of 1α,25(OH)(2)-3-epi-D(3) and its receptor complex, we characterized some of its in vitro biological properties and solved its crystal structure complexed with human VDR ligand-binding domain (LBD). METHODOLOGY/PRINCIPAL FINDINGS: In the present study, we report the more effective synthesis with fewer steps that provides higher yield of the 3-epimer of the 1α,25(OH)(2)D(3). We solved the crystal structure of its complex with the human VDR-LBD and found that this natural metabolite displays specific adaptation of the ligand-binding pocket, as the 3-epimer maintains the number of hydrogen bonds by an alternative water-mediated interaction to compensate the abolished interaction with Ser278. In addition, the biological activity of the 1α,25(OH)(2)-3-epi-D(3) in primary human keratinocytes and biochemical properties are comparable to 1α,25(OH)(2)D(3). CONCLUSIONS/SIGNIFICANCE: The physiological role of this pathway as the specific biological action of the 3-epimer remains unclear. However, its high metabolic stability together with its significant biologic activity makes this natural metabolite an interesting ligand for clinical applications. Our new findings contribute to a better understanding at molecular level how natural metabolites of 1α,25(OH)(2)D(3) lead to significant activity in biological systems and we conclude that the C3-epimerization pathway produces an active metabolite with similar biochemical and biological properties to those of the 1α,25(OH)(2)D(3). Public Library of Science 2011-03-31 /pmc/articles/PMC3069065/ /pubmed/21483824 http://dx.doi.org/10.1371/journal.pone.0018124 Text en Molnár et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Molnár, Ferdinand Sigüeiro, Rita Sato, Yoshiteru Araujo, Clarisse Schuster, Inge Antony, Pierre Peluso, Jean Muller, Christian Mouriño, Antonio Moras, Dino Rochel, Natacha 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor |
title | 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor |
title_full | 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor |
title_fullStr | 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor |
title_full_unstemmed | 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor |
title_short | 1α,25(OH)(2)-3-Epi-Vitamin D(3), a Natural Physiological Metabolite of Vitamin D(3): Its Synthesis, Biological Activity and Crystal Structure with Its Receptor |
title_sort | 1α,25(oh)(2)-3-epi-vitamin d(3), a natural physiological metabolite of vitamin d(3): its synthesis, biological activity and crystal structure with its receptor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069065/ https://www.ncbi.nlm.nih.gov/pubmed/21483824 http://dx.doi.org/10.1371/journal.pone.0018124 |
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