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Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis
The M3 metalloproteases, neurolysin and THOP1, are neuropeptidases that are expressed in various tissues and metabolize neuropeptides, such as neurotensin. The biological roles of these enzymes are not well characterized, partially because the chemical tools to analyse their activities are not well...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155908/ https://www.ncbi.nlm.nih.gov/pubmed/37152255 http://dx.doi.org/10.1039/d2sc07029d |
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author | Nagano, Norimichi Ichihashi, Yuki Komatsu, Toru Matsuzaki, Hiroyuki Hata, Keisuke Watanabe, Toshiaki Misawa, Yoshihiro Suzuki, Misa Sakamoto, Shingo Kagami, Yu Kashiro, Ayumi Takeuchi, Keiko Kanemitsu, Yukihide Ochiai, Hiroki Watanabe, Rikiya Honda, Kazufumi Urano, Yasuteru |
author_facet | Nagano, Norimichi Ichihashi, Yuki Komatsu, Toru Matsuzaki, Hiroyuki Hata, Keisuke Watanabe, Toshiaki Misawa, Yoshihiro Suzuki, Misa Sakamoto, Shingo Kagami, Yu Kashiro, Ayumi Takeuchi, Keiko Kanemitsu, Yukihide Ochiai, Hiroki Watanabe, Rikiya Honda, Kazufumi Urano, Yasuteru |
author_sort | Nagano, Norimichi |
collection | PubMed |
description | The M3 metalloproteases, neurolysin and THOP1, are neuropeptidases that are expressed in various tissues and metabolize neuropeptides, such as neurotensin. The biological roles of these enzymes are not well characterized, partially because the chemical tools to analyse their activities are not well developed. Here, we developed a fluorogenic substrate probe for neurolysin and thimet oligopeptidase 1 (THOP1), which enabled the analysis of enzymatic activity changes in tissue and plasma samples. In particular, the probe was useful for studying enzyme activities in a single-molecule enzyme assay platform, which can detect enzyme activity with high sensitivity. We detected the activity of neurolysin in plasma samples and revealed higher enzyme activity in the blood samples of patients with colorectal tumor. The result indicated that single-molecule neurolysin activity is a promising candidate for a blood biomarker for colorectal cancer diagnosis. |
format | Online Article Text |
id | pubmed-10155908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-101559082023-05-04 Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis Nagano, Norimichi Ichihashi, Yuki Komatsu, Toru Matsuzaki, Hiroyuki Hata, Keisuke Watanabe, Toshiaki Misawa, Yoshihiro Suzuki, Misa Sakamoto, Shingo Kagami, Yu Kashiro, Ayumi Takeuchi, Keiko Kanemitsu, Yukihide Ochiai, Hiroki Watanabe, Rikiya Honda, Kazufumi Urano, Yasuteru Chem Sci Chemistry The M3 metalloproteases, neurolysin and THOP1, are neuropeptidases that are expressed in various tissues and metabolize neuropeptides, such as neurotensin. The biological roles of these enzymes are not well characterized, partially because the chemical tools to analyse their activities are not well developed. Here, we developed a fluorogenic substrate probe for neurolysin and thimet oligopeptidase 1 (THOP1), which enabled the analysis of enzymatic activity changes in tissue and plasma samples. In particular, the probe was useful for studying enzyme activities in a single-molecule enzyme assay platform, which can detect enzyme activity with high sensitivity. We detected the activity of neurolysin in plasma samples and revealed higher enzyme activity in the blood samples of patients with colorectal tumor. The result indicated that single-molecule neurolysin activity is a promising candidate for a blood biomarker for colorectal cancer diagnosis. The Royal Society of Chemistry 2023-04-11 /pmc/articles/PMC10155908/ /pubmed/37152255 http://dx.doi.org/10.1039/d2sc07029d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Nagano, Norimichi Ichihashi, Yuki Komatsu, Toru Matsuzaki, Hiroyuki Hata, Keisuke Watanabe, Toshiaki Misawa, Yoshihiro Suzuki, Misa Sakamoto, Shingo Kagami, Yu Kashiro, Ayumi Takeuchi, Keiko Kanemitsu, Yukihide Ochiai, Hiroki Watanabe, Rikiya Honda, Kazufumi Urano, Yasuteru Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
title | Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
title_full | Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
title_fullStr | Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
title_full_unstemmed | Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
title_short | Development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
title_sort | development of fluorogenic substrates for colorectal tumor-related neuropeptidases for activity-based diagnosis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155908/ https://www.ncbi.nlm.nih.gov/pubmed/37152255 http://dx.doi.org/10.1039/d2sc07029d |
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