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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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