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Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity
Dipeptidyl peptidase-4 inhibitors (DPP4i) are a class of orally available, small molecule inhibitors for the management of Type-II diabetes. A rapid, real-time, functional breath test for DPP4 enzyme activity could help to define DPP4i efficacy in patients that are refractory to treatment. We aimed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427020/ https://www.ncbi.nlm.nih.gov/pubmed/30894647 http://dx.doi.org/10.1038/s41598-019-41375-y |
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author | Yazbeck, Roger Jaenisch, Simone Squire, Michelle Abbott, Catherine A. Parkinson-Lawrence, Emma Brooks, Douglas A. Butler, Ross N. |
author_facet | Yazbeck, Roger Jaenisch, Simone Squire, Michelle Abbott, Catherine A. Parkinson-Lawrence, Emma Brooks, Douglas A. Butler, Ross N. |
author_sort | Yazbeck, Roger |
collection | PubMed |
description | Dipeptidyl peptidase-4 inhibitors (DPP4i) are a class of orally available, small molecule inhibitors for the management of Type-II diabetes. A rapid, real-time, functional breath test for DPP4 enzyme activity could help to define DPP4i efficacy in patients that are refractory to treatment. We aimed to develop a selective, non-invasive, stable-isotope (13)C-breath test for DPP4. In vitro experiments were performed using high (Caco-2) and low (HeLa) DPP4 expressing cells. DPP gene expression was determined in cell lines by qRT-PCR. A DPP4 selective (13)C-tripeptide was added to cells in the presence and absence of the DPP4 inhibitor Sitagliptin. Gas samples were collected from the cell headspace and (13)CO(2) content quantified by isotope ratio mass spectrometry (IRMS). DPP4 was highly expressed in Caco-2 cells compared to HeLa cells and using the (13)C-tripeptide, we detected a high (13)CO(2) signal from Caco2 cells. Addition of Sitaglitpin to Caco2 cells significantly inhibited this (13)CO(2) signal. (13)C-assay DPP4 activity correlated positively with the enzyme activity detected using a colorimetric substrate. We have developed a selective, non-invasive, (13)C-assay for DPP4 that could have broad translational applications in diabetes and gastrointestinal disease. |
format | Online Article Text |
id | pubmed-6427020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64270202019-03-28 Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity Yazbeck, Roger Jaenisch, Simone Squire, Michelle Abbott, Catherine A. Parkinson-Lawrence, Emma Brooks, Douglas A. Butler, Ross N. Sci Rep Article Dipeptidyl peptidase-4 inhibitors (DPP4i) are a class of orally available, small molecule inhibitors for the management of Type-II diabetes. A rapid, real-time, functional breath test for DPP4 enzyme activity could help to define DPP4i efficacy in patients that are refractory to treatment. We aimed to develop a selective, non-invasive, stable-isotope (13)C-breath test for DPP4. In vitro experiments were performed using high (Caco-2) and low (HeLa) DPP4 expressing cells. DPP gene expression was determined in cell lines by qRT-PCR. A DPP4 selective (13)C-tripeptide was added to cells in the presence and absence of the DPP4 inhibitor Sitagliptin. Gas samples were collected from the cell headspace and (13)CO(2) content quantified by isotope ratio mass spectrometry (IRMS). DPP4 was highly expressed in Caco-2 cells compared to HeLa cells and using the (13)C-tripeptide, we detected a high (13)CO(2) signal from Caco2 cells. Addition of Sitaglitpin to Caco2 cells significantly inhibited this (13)CO(2) signal. (13)C-assay DPP4 activity correlated positively with the enzyme activity detected using a colorimetric substrate. We have developed a selective, non-invasive, (13)C-assay for DPP4 that could have broad translational applications in diabetes and gastrointestinal disease. Nature Publishing Group UK 2019-03-20 /pmc/articles/PMC6427020/ /pubmed/30894647 http://dx.doi.org/10.1038/s41598-019-41375-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yazbeck, Roger Jaenisch, Simone Squire, Michelle Abbott, Catherine A. Parkinson-Lawrence, Emma Brooks, Douglas A. Butler, Ross N. Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity |
title | Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity |
title_full | Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity |
title_fullStr | Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity |
title_full_unstemmed | Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity |
title_short | Development of a (13)C Stable Isotope Assay for Dipeptidyl Peptidase-4 Enzyme Activity A New Breath Test for Dipeptidyl Peptidase Activity |
title_sort | development of a (13)c stable isotope assay for dipeptidyl peptidase-4 enzyme activity a new breath test for dipeptidyl peptidase activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427020/ https://www.ncbi.nlm.nih.gov/pubmed/30894647 http://dx.doi.org/10.1038/s41598-019-41375-y |
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