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In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application
A lectin-like protein of unknown function designated as LSMT was recently discovered in the edible mushroom Agaricus bisporus. The protein shares high structural similarity to HA-33 from Clostridium botulinum (HA33) and Ricin-B-like lectin from the mushroom Clitocybe nebularis (CNL), which have been...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Austrian Journal of Pharmaceutical Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839548/ https://www.ncbi.nlm.nih.gov/pubmed/27110510 http://dx.doi.org/10.3797/scipharm.ISP.2015.11 |
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author | Ismaya, Wangsa Tirta Yunita, Damayanti, Sophi Wijaya, Caroline Tjandrawinata, Raymond R. Retnoningrum, Debbie Sofie Rachmawati, Heni |
author_facet | Ismaya, Wangsa Tirta Yunita, Damayanti, Sophi Wijaya, Caroline Tjandrawinata, Raymond R. Retnoningrum, Debbie Sofie Rachmawati, Heni |
author_sort | Ismaya, Wangsa Tirta |
collection | PubMed |
description | A lectin-like protein of unknown function designated as LSMT was recently discovered in the edible mushroom Agaricus bisporus. The protein shares high structural similarity to HA-33 from Clostridium botulinum (HA33) and Ricin-B-like lectin from the mushroom Clitocybe nebularis (CNL), which have been developed as drug carrier and anti-cancer, respectively. These homologous proteins display the ability to penetrate the intestinal epithelial cell monolayer, and are beneficial for oral administration. As the characteristics of LSMT are unknown, a structural study in silico was performed to assess its potential pharmaceutical application. The study suggested potential binding to target ligands such as HA-33 and CNL although the nature, specificity, capacity, mode, and strength may differ. Further molecular docking experiments suggest that interactions between the LSMT and tested ligands may take place. This finding indicates the possible use of the LSMT protein, initiating new research on its use for pharmaceutical purposes. |
format | Online Article Text |
id | pubmed-4839548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Austrian Journal of Pharmaceutical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-48395482016-04-22 In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application Ismaya, Wangsa Tirta Yunita, Damayanti, Sophi Wijaya, Caroline Tjandrawinata, Raymond R. Retnoningrum, Debbie Sofie Rachmawati, Heni Sci Pharm Conference Article A lectin-like protein of unknown function designated as LSMT was recently discovered in the edible mushroom Agaricus bisporus. The protein shares high structural similarity to HA-33 from Clostridium botulinum (HA33) and Ricin-B-like lectin from the mushroom Clitocybe nebularis (CNL), which have been developed as drug carrier and anti-cancer, respectively. These homologous proteins display the ability to penetrate the intestinal epithelial cell monolayer, and are beneficial for oral administration. As the characteristics of LSMT are unknown, a structural study in silico was performed to assess its potential pharmaceutical application. The study suggested potential binding to target ligands such as HA-33 and CNL although the nature, specificity, capacity, mode, and strength may differ. Further molecular docking experiments suggest that interactions between the LSMT and tested ligands may take place. This finding indicates the possible use of the LSMT protein, initiating new research on its use for pharmaceutical purposes. The Austrian Journal of Pharmaceutical Sciences 2016 2016-02-14 /pmc/articles/PMC4839548/ /pubmed/27110510 http://dx.doi.org/10.3797/scipharm.ISP.2015.11 Text en Copyright: © Ismaya et al. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Conference Article Ismaya, Wangsa Tirta Yunita, Damayanti, Sophi Wijaya, Caroline Tjandrawinata, Raymond R. Retnoningrum, Debbie Sofie Rachmawati, Heni In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application |
title | In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application |
title_full | In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application |
title_fullStr | In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application |
title_full_unstemmed | In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application |
title_short | In Silico Study to Develop a Lectin-Like Protein from Mushroom Agaricus bisporus for Pharmaceutical Application |
title_sort | in silico study to develop a lectin-like protein from mushroom agaricus bisporus for pharmaceutical application |
topic | Conference Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839548/ https://www.ncbi.nlm.nih.gov/pubmed/27110510 http://dx.doi.org/10.3797/scipharm.ISP.2015.11 |
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