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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...

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Autores principales: Nakano, Shogo, Megro, Shin-ichi, Hase, Tadashi, Suzuki, Takuji, Isemura, Mamoru, Nakamura, Yoriyuki, Ito, Sohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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