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EFR3A: a new raft domain organizing protein?
BACKGROUND: Membrane rafts play a crucial role in the regulation of many important biological processes. Our previous data suggest that specific interactions of flotillins with MPP1 are responsible for membrane raft domain organization and regulation in erythroid cells. Interaction of the flotillin-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601247/ https://www.ncbi.nlm.nih.gov/pubmed/37880612 http://dx.doi.org/10.1186/s11658-023-00497-y |
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author | Trybus, Magdalena Hryniewicz-Jankowska, Anita Wójtowicz, Karolina Trombik, Tomasz Czogalla, Aleksander Sikorski, Aleksander F. |
author_facet | Trybus, Magdalena Hryniewicz-Jankowska, Anita Wójtowicz, Karolina Trombik, Tomasz Czogalla, Aleksander Sikorski, Aleksander F. |
author_sort | Trybus, Magdalena |
collection | PubMed |
description | BACKGROUND: Membrane rafts play a crucial role in the regulation of many important biological processes. Our previous data suggest that specific interactions of flotillins with MPP1 are responsible for membrane raft domain organization and regulation in erythroid cells. Interaction of the flotillin-based protein network with specific membrane components underlies the mechanism of raft domain formation and regulation, including in cells with low expression of MPP1. METHODS: We sought to identify other flotillin partners via the immobilized recombinant flotillin-2-based affinity approach and mass spectrometry technique. The results were further confirmed via immunoblotting and via co-immunoprecipitation. In order to study the effect of the candidate protein on the physicochemical properties of the plasma membrane, the gene was knocked down via siRNA, and fluorescence lifetime imaging microscopy and spot-variation fluorescence correlation spectroscopy was employed. RESULTS: EFR3A was identified as a candidate protein that interacts with flotillin-2. Moreover, this newly discovered interaction was demonstrated via overlay assay using recombinant EFR3A and flotillin-2. EFR3A is a stable component of the detergent-resistant membrane fraction of HeLa cells, and its presence was sensitive to the removal of cholesterol. While silencing the EFR3A gene, we observed decreased order of the plasma membrane of living cells or giant plasma membrane vesicles derived from knocked down cells and altered mobility of the raft probe, as indicated via fluorescence lifetime imaging microscopy and spot-variation fluorescence correlation spectroscopy. Moreover, silencing of EFR3A expression was found to disturb epidermal growth factor receptor and phospholipase C gamma phosphorylation and affect epidermal growth factor-dependent cytosolic Ca(2+) concentration. CONCLUSIONS: Altogether, our results suggest hitherto unreported flotillin-2-EFR3A interaction, which might be responsible for membrane raft organization and regulation. This implies participation of this interaction in the regulation of multiple cellular processes, including those connected with cell signaling which points to the possible role in human health, in particular human cancer biology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11658-023-00497-y. |
format | Online Article Text |
id | pubmed-10601247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106012472023-10-27 EFR3A: a new raft domain organizing protein? Trybus, Magdalena Hryniewicz-Jankowska, Anita Wójtowicz, Karolina Trombik, Tomasz Czogalla, Aleksander Sikorski, Aleksander F. Cell Mol Biol Lett Research BACKGROUND: Membrane rafts play a crucial role in the regulation of many important biological processes. Our previous data suggest that specific interactions of flotillins with MPP1 are responsible for membrane raft domain organization and regulation in erythroid cells. Interaction of the flotillin-based protein network with specific membrane components underlies the mechanism of raft domain formation and regulation, including in cells with low expression of MPP1. METHODS: We sought to identify other flotillin partners via the immobilized recombinant flotillin-2-based affinity approach and mass spectrometry technique. The results were further confirmed via immunoblotting and via co-immunoprecipitation. In order to study the effect of the candidate protein on the physicochemical properties of the plasma membrane, the gene was knocked down via siRNA, and fluorescence lifetime imaging microscopy and spot-variation fluorescence correlation spectroscopy was employed. RESULTS: EFR3A was identified as a candidate protein that interacts with flotillin-2. Moreover, this newly discovered interaction was demonstrated via overlay assay using recombinant EFR3A and flotillin-2. EFR3A is a stable component of the detergent-resistant membrane fraction of HeLa cells, and its presence was sensitive to the removal of cholesterol. While silencing the EFR3A gene, we observed decreased order of the plasma membrane of living cells or giant plasma membrane vesicles derived from knocked down cells and altered mobility of the raft probe, as indicated via fluorescence lifetime imaging microscopy and spot-variation fluorescence correlation spectroscopy. Moreover, silencing of EFR3A expression was found to disturb epidermal growth factor receptor and phospholipase C gamma phosphorylation and affect epidermal growth factor-dependent cytosolic Ca(2+) concentration. CONCLUSIONS: Altogether, our results suggest hitherto unreported flotillin-2-EFR3A interaction, which might be responsible for membrane raft organization and regulation. This implies participation of this interaction in the regulation of multiple cellular processes, including those connected with cell signaling which points to the possible role in human health, in particular human cancer biology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11658-023-00497-y. BioMed Central 2023-10-25 /pmc/articles/PMC10601247/ /pubmed/37880612 http://dx.doi.org/10.1186/s11658-023-00497-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Trybus, Magdalena Hryniewicz-Jankowska, Anita Wójtowicz, Karolina Trombik, Tomasz Czogalla, Aleksander Sikorski, Aleksander F. EFR3A: a new raft domain organizing protein? |
title | EFR3A: a new raft domain organizing protein? |
title_full | EFR3A: a new raft domain organizing protein? |
title_fullStr | EFR3A: a new raft domain organizing protein? |
title_full_unstemmed | EFR3A: a new raft domain organizing protein? |
title_short | EFR3A: a new raft domain organizing protein? |
title_sort | efr3a: a new raft domain organizing protein? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601247/ https://www.ncbi.nlm.nih.gov/pubmed/37880612 http://dx.doi.org/10.1186/s11658-023-00497-y |
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