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Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH
Enzymes are regulated by their activation and inhibition. Enzyme activators can often be effective tools for scientific and medical purposes, although they are more difficult to obtain than inhibitors. Here, using the paired peptide method, we report on protease-cathepsin-E-activating peptides that...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534310/ https://www.ncbi.nlm.nih.gov/pubmed/23365585 http://dx.doi.org/10.1155/2012/316432 |
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author | Komatsu, Masayuki Biyani, Madhu Ghimire Gautam, Sunita Nishigaki, Koichi |
author_facet | Komatsu, Masayuki Biyani, Madhu Ghimire Gautam, Sunita Nishigaki, Koichi |
author_sort | Komatsu, Masayuki |
collection | PubMed |
description | Enzymes are regulated by their activation and inhibition. Enzyme activators can often be effective tools for scientific and medical purposes, although they are more difficult to obtain than inhibitors. Here, using the paired peptide method, we report on protease-cathepsin-E-activating peptides that are obtained at neutral pH. These selected peptides also underwent molecular evolution, after which their cathepsin E activation capability improved. Thus, the activators we obtained could enhance cathepsin-E-induced cancer cell apoptosis, which indicated their potential as cancer drug precursors. |
format | Online Article Text |
id | pubmed-3534310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35343102013-01-30 Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH Komatsu, Masayuki Biyani, Madhu Ghimire Gautam, Sunita Nishigaki, Koichi Int J Pept Research Article Enzymes are regulated by their activation and inhibition. Enzyme activators can often be effective tools for scientific and medical purposes, although they are more difficult to obtain than inhibitors. Here, using the paired peptide method, we report on protease-cathepsin-E-activating peptides that are obtained at neutral pH. These selected peptides also underwent molecular evolution, after which their cathepsin E activation capability improved. Thus, the activators we obtained could enhance cathepsin-E-induced cancer cell apoptosis, which indicated their potential as cancer drug precursors. Hindawi Publishing Corporation 2012 2012-12-17 /pmc/articles/PMC3534310/ /pubmed/23365585 http://dx.doi.org/10.1155/2012/316432 Text en Copyright © 2012 Masayuki Komatsu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Komatsu, Masayuki Biyani, Madhu Ghimire Gautam, Sunita Nishigaki, Koichi Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH |
title | Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH |
title_full | Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH |
title_fullStr | Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH |
title_full_unstemmed | Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH |
title_short | Peptide-Modulated Activity Enhancement of Acidic Protease Cathepsin E at Neutral pH |
title_sort | peptide-modulated activity enhancement of acidic protease cathepsin e at neutral ph |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534310/ https://www.ncbi.nlm.nih.gov/pubmed/23365585 http://dx.doi.org/10.1155/2012/316432 |
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