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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...

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Autores principales: Lin, Weilin, Bonin, Malte, Boden, Annett, Wieduwild, Robert, Murawala, Priyanka, Wermke, Martin, Andrade, Helena, Bornhäuser, Martin, Zhang, Yixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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