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Comparative molecular docking analysis of essential oil constituents as elastase inhibitors
Elastase is a protease or proteolytic enzyme, responsible for the breakdown of protein. There are eight human genes encoding for elastase, of which Elastase-1 (CELA-1) and Elastase-2 (ELANE) has significant implications on human diseases. Elastase-1 is primarily expressed in skin keratinocytes and i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Biomedical Informatics
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374355/ https://www.ncbi.nlm.nih.gov/pubmed/22715299 http://dx.doi.org/10.6026/97320630008457 |
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author | Sivamani, Periyasamy Singaravelu, Ganesan Thiagarajan, Venkatesan Jayalakshmi, Tamilarasu Ramesh Kumar, Gopal |
author_facet | Sivamani, Periyasamy Singaravelu, Ganesan Thiagarajan, Venkatesan Jayalakshmi, Tamilarasu Ramesh Kumar, Gopal |
author_sort | Sivamani, Periyasamy |
collection | PubMed |
description | Elastase is a protease or proteolytic enzyme, responsible for the breakdown of protein. There are eight human genes encoding for elastase, of which Elastase-1 (CELA-1) and Elastase-2 (ELANE) has significant implications on human diseases. Elastase-1 is primarily expressed in skin keratinocytes and is regarded as the major cause for the blistering in bullous pemphigoid, which affects the skin. On the other hand, Elastase-2 (ELANE), is expressed in the azurophil granules of neutrophils, is responsible for pulmonary emphysema and cyclic hematopoiesis a rare genetic disorder. Elastase is also produced by bacteria such as Pseudomonas aeruginosa, and forms the virulent factor in human. The ingredients from essential natural oils were found to have wound healing effects on non-healing wounds that is interfered by elastase due to microbial infection. Essential oils such as citral, citronellal, geranial, geraniol, and thymol were screened for their inhibitory activity on elastase produced by neutrophil, skin, and Pseudomonas aeruginosa by docking and were analyzed for their subcutaneous ADMET properties by ADME – TOX – Web server. |
format | Online Article Text |
id | pubmed-3374355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-33743552012-06-19 Comparative molecular docking analysis of essential oil constituents as elastase inhibitors Sivamani, Periyasamy Singaravelu, Ganesan Thiagarajan, Venkatesan Jayalakshmi, Tamilarasu Ramesh Kumar, Gopal Bioinformation Hypothesis Elastase is a protease or proteolytic enzyme, responsible for the breakdown of protein. There are eight human genes encoding for elastase, of which Elastase-1 (CELA-1) and Elastase-2 (ELANE) has significant implications on human diseases. Elastase-1 is primarily expressed in skin keratinocytes and is regarded as the major cause for the blistering in bullous pemphigoid, which affects the skin. On the other hand, Elastase-2 (ELANE), is expressed in the azurophil granules of neutrophils, is responsible for pulmonary emphysema and cyclic hematopoiesis a rare genetic disorder. Elastase is also produced by bacteria such as Pseudomonas aeruginosa, and forms the virulent factor in human. The ingredients from essential natural oils were found to have wound healing effects on non-healing wounds that is interfered by elastase due to microbial infection. Essential oils such as citral, citronellal, geranial, geraniol, and thymol were screened for their inhibitory activity on elastase produced by neutrophil, skin, and Pseudomonas aeruginosa by docking and were analyzed for their subcutaneous ADMET properties by ADME – TOX – Web server. Biomedical Informatics 2012-05-31 /pmc/articles/PMC3374355/ /pubmed/22715299 http://dx.doi.org/10.6026/97320630008457 Text en © 2012 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Hypothesis Sivamani, Periyasamy Singaravelu, Ganesan Thiagarajan, Venkatesan Jayalakshmi, Tamilarasu Ramesh Kumar, Gopal Comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
title | Comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
title_full | Comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
title_fullStr | Comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
title_full_unstemmed | Comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
title_short | Comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
title_sort | comparative molecular docking analysis of essential oil constituents as elastase inhibitors |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374355/ https://www.ncbi.nlm.nih.gov/pubmed/22715299 http://dx.doi.org/10.6026/97320630008457 |
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