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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...

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Autores principales: Komatsu, Masayuki, Biyani, Madhu, Ghimire Gautam, Sunita, Nishigaki, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
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.
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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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