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Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies
Epidemiological and laboratory studies have shown that green tea and green tea catechins exert beneficial effects on a variety of diseases, including cancer, metabolic syndrome, infectious diseases, and neurodegenerative diseases. In most cases, (−)-epigallocatechin gallate (EGCG) has been shown to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222539/ https://www.ncbi.nlm.nih.gov/pubmed/30104534 http://dx.doi.org/10.3390/molecules23082020 |
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author | Nakano, Shogo Megro, Shin-ichi Hase, Tadashi Suzuki, Takuji Isemura, Mamoru Nakamura, Yoriyuki Ito, Sohei |
author_facet | Nakano, Shogo Megro, Shin-ichi Hase, Tadashi Suzuki, Takuji Isemura, Mamoru Nakamura, Yoriyuki Ito, Sohei |
author_sort | Nakano, Shogo |
collection | PubMed |
description | Epidemiological and laboratory studies have shown that green tea and green tea catechins exert beneficial effects on a variety of diseases, including cancer, metabolic syndrome, infectious diseases, and neurodegenerative diseases. In most cases, (−)-epigallocatechin gallate (EGCG) has been shown to play a central role in these effects by green tea. Catechins from other plant sources have also shown health benefits. Many studies have revealed that the binding of EGCG and other catechins to proteins is involved in its action mechanism. Computational docking analysis (CMDA) and X-ray crystallographic analysis (XCA) have provided detailed information on catechin-protein interactions. Several of these studies have revealed that the galloyl moiety anchors it to the cleft of proteins through interactions with its hydroxyl groups, explaining the higher activity of galloylated catechins such as EGCG and epicatechin gallate than non-galloylated catechins. In this paper, we review the results of CMDA and XCA of EGCG and other plant catechins to understand catechin-protein interactions with the expectation of developing new drugs with health-promoting properties. |
format | Online Article Text |
id | pubmed-6222539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62225392018-11-13 Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies Nakano, Shogo Megro, Shin-ichi Hase, Tadashi Suzuki, Takuji Isemura, Mamoru Nakamura, Yoriyuki Ito, Sohei Molecules Review Epidemiological and laboratory studies have shown that green tea and green tea catechins exert beneficial effects on a variety of diseases, including cancer, metabolic syndrome, infectious diseases, and neurodegenerative diseases. In most cases, (−)-epigallocatechin gallate (EGCG) has been shown to play a central role in these effects by green tea. Catechins from other plant sources have also shown health benefits. Many studies have revealed that the binding of EGCG and other catechins to proteins is involved in its action mechanism. Computational docking analysis (CMDA) and X-ray crystallographic analysis (XCA) have provided detailed information on catechin-protein interactions. Several of these studies have revealed that the galloyl moiety anchors it to the cleft of proteins through interactions with its hydroxyl groups, explaining the higher activity of galloylated catechins such as EGCG and epicatechin gallate than non-galloylated catechins. In this paper, we review the results of CMDA and XCA of EGCG and other plant catechins to understand catechin-protein interactions with the expectation of developing new drugs with health-promoting properties. MDPI 2018-08-13 /pmc/articles/PMC6222539/ /pubmed/30104534 http://dx.doi.org/10.3390/molecules23082020 Text en © 2018 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 | Review Nakano, Shogo Megro, Shin-ichi Hase, Tadashi Suzuki, Takuji Isemura, Mamoru Nakamura, Yoriyuki Ito, Sohei Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies |
title | Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies |
title_full | Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies |
title_fullStr | Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies |
title_full_unstemmed | Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies |
title_short | Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies |
title_sort | computational molecular docking and x-ray crystallographic studies of catechins in new drug design strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222539/ https://www.ncbi.nlm.nih.gov/pubmed/30104534 http://dx.doi.org/10.3390/molecules23082020 |
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