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Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development
Interactions with the extracellular matrix (ECM) dictate cell fates. However, the complexity of dense ECM network and cell-surface molecules prevent the study of their dynamic interaction at the molecular level on living cells. Here, we focus on peptidyl prolyl cis/trans isomerases (PPIases) to diss...
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/PMC6370856/ https://www.ncbi.nlm.nih.gov/pubmed/30775459 http://dx.doi.org/10.1038/s42003-019-0315-8 |
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author | Lin, Weilin Bonin, Malte Boden, Annett Wieduwild, Robert Murawala, Priyanka Wermke, Martin Andrade, Helena Bornhäuser, Martin Zhang, Yixin |
author_facet | Lin, Weilin Bonin, Malte Boden, Annett Wieduwild, Robert Murawala, Priyanka Wermke, Martin Andrade, Helena Bornhäuser, Martin Zhang, Yixin |
author_sort | Lin, Weilin |
collection | PubMed |
description | Interactions with the extracellular matrix (ECM) dictate cell fates. However, the complexity of dense ECM network and cell-surface molecules prevent the study of their dynamic interaction at the molecular level on living cells. Here, we focus on peptidyl prolyl cis/trans isomerases (PPIases) to dissect prolyl isomerization from other dynamic events. We reveal the contribution of PPIase on the mechanical properties of various ECM materials and on the dynamic cell–ECM interaction. To avoid complications associated with the existing spectroscopy-based methods such as light scattering, an assay was developed for detecting PPIase activity on living cell surface. This assay allows us to correlate PPIase activity with ECM development, and with the physiological and pathological states of the cells, including the functional properties of cancer cells and immune effector cells. |
format | Online Article Text |
id | pubmed-6370856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63708562019-02-15 Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development Lin, Weilin Bonin, Malte Boden, Annett Wieduwild, Robert Murawala, Priyanka Wermke, Martin Andrade, Helena Bornhäuser, Martin Zhang, Yixin Commun Biol Article Interactions with the extracellular matrix (ECM) dictate cell fates. However, the complexity of dense ECM network and cell-surface molecules prevent the study of their dynamic interaction at the molecular level on living cells. Here, we focus on peptidyl prolyl cis/trans isomerases (PPIases) to dissect prolyl isomerization from other dynamic events. We reveal the contribution of PPIase on the mechanical properties of various ECM materials and on the dynamic cell–ECM interaction. To avoid complications associated with the existing spectroscopy-based methods such as light scattering, an assay was developed for detecting PPIase activity on living cell surface. This assay allows us to correlate PPIase activity with ECM development, and with the physiological and pathological states of the cells, including the functional properties of cancer cells and immune effector cells. Nature Publishing Group UK 2019-02-11 /pmc/articles/PMC6370856/ /pubmed/30775459 http://dx.doi.org/10.1038/s42003-019-0315-8 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 Lin, Weilin Bonin, Malte Boden, Annett Wieduwild, Robert Murawala, Priyanka Wermke, Martin Andrade, Helena Bornhäuser, Martin Zhang, Yixin Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
title | Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
title_full | Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
title_fullStr | Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
title_full_unstemmed | Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
title_short | Peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
title_sort | peptidyl prolyl cis/trans isomerase activity on the cell surface correlates with extracellular matrix development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370856/ https://www.ncbi.nlm.nih.gov/pubmed/30775459 http://dx.doi.org/10.1038/s42003-019-0315-8 |
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