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Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding
PTEN, a 3-phosphatase of phosphoinositide, regulates asymmetric PI(3,4,5)P(3) signaling for the anterior-posterior polarization and migration of motile cells. PTEN acts through posterior localization on the plasma membrane, but the mechanism for this accumulation is poorly understood. Here we develo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048775/ https://www.ncbi.nlm.nih.gov/pubmed/32111929 http://dx.doi.org/10.1038/s42003-020-0818-3 |
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author | Yoshioka, Daisuke Fukushima, Seiya Koteishi, Hiroyasu Okuno, Daichi Ide, Toru Matsuoka, Satomi Ueda, Masahiro |
author_facet | Yoshioka, Daisuke Fukushima, Seiya Koteishi, Hiroyasu Okuno, Daichi Ide, Toru Matsuoka, Satomi Ueda, Masahiro |
author_sort | Yoshioka, Daisuke |
collection | PubMed |
description | PTEN, a 3-phosphatase of phosphoinositide, regulates asymmetric PI(3,4,5)P(3) signaling for the anterior-posterior polarization and migration of motile cells. PTEN acts through posterior localization on the plasma membrane, but the mechanism for this accumulation is poorly understood. Here we developed an in vitro single-molecule imaging assay with various lipid compositions and use it to demonstrate that the enzymatic product, PI(4,5)P(2), stabilizes PTEN’s membrane-binding. The dissociation kinetics and lateral mobility of PTEN depended on the PI(4,5)P(2) density on artificial lipid bilayers. The basic residues of PTEN were responsible for electrostatic interactions with anionic PI(4,5)P(2) and thus the PI(4,5)P(2)-dependent stabilization. Single-molecule imaging in living Dictyostelium cells revealed that these interactions were indispensable for the stabilization in vivo, which enabled efficient cell migration by accumulating PTEN posteriorly to restrict PI(3,4,5)P(3) distribution to the anterior. These results suggest that PI(4,5)P(2)-mediated positive feedback and PTEN-induced PI(4,5)P(2) clustering may be important for anterior-posterior polarization. |
format | Online Article Text |
id | pubmed-7048775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70487752020-03-05 Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding Yoshioka, Daisuke Fukushima, Seiya Koteishi, Hiroyasu Okuno, Daichi Ide, Toru Matsuoka, Satomi Ueda, Masahiro Commun Biol Article PTEN, a 3-phosphatase of phosphoinositide, regulates asymmetric PI(3,4,5)P(3) signaling for the anterior-posterior polarization and migration of motile cells. PTEN acts through posterior localization on the plasma membrane, but the mechanism for this accumulation is poorly understood. Here we developed an in vitro single-molecule imaging assay with various lipid compositions and use it to demonstrate that the enzymatic product, PI(4,5)P(2), stabilizes PTEN’s membrane-binding. The dissociation kinetics and lateral mobility of PTEN depended on the PI(4,5)P(2) density on artificial lipid bilayers. The basic residues of PTEN were responsible for electrostatic interactions with anionic PI(4,5)P(2) and thus the PI(4,5)P(2)-dependent stabilization. Single-molecule imaging in living Dictyostelium cells revealed that these interactions were indispensable for the stabilization in vivo, which enabled efficient cell migration by accumulating PTEN posteriorly to restrict PI(3,4,5)P(3) distribution to the anterior. These results suggest that PI(4,5)P(2)-mediated positive feedback and PTEN-induced PI(4,5)P(2) clustering may be important for anterior-posterior polarization. Nature Publishing Group UK 2020-02-28 /pmc/articles/PMC7048775/ /pubmed/32111929 http://dx.doi.org/10.1038/s42003-020-0818-3 Text en © The Author(s) 2020 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 Yoshioka, Daisuke Fukushima, Seiya Koteishi, Hiroyasu Okuno, Daichi Ide, Toru Matsuoka, Satomi Ueda, Masahiro Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding |
title | Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding |
title_full | Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding |
title_fullStr | Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding |
title_full_unstemmed | Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding |
title_short | Single-molecule imaging of PI(4,5)P(2) and PTEN in vitro reveals a positive feedback mechanism for PTEN membrane binding |
title_sort | single-molecule imaging of pi(4,5)p(2) and pten in vitro reveals a positive feedback mechanism for pten membrane binding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048775/ https://www.ncbi.nlm.nih.gov/pubmed/32111929 http://dx.doi.org/10.1038/s42003-020-0818-3 |
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