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Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein
The higher-order assembly of Bin-amphiphysin-Rvs (BAR) domain proteins, including the FCH-BAR (F-BAR) domain proteins, into lattice on the membrane is essential for the formation of subcellular structures. However, the regulation of their ordered assembly has not been elucidated. Here, we show that...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132759/ https://www.ncbi.nlm.nih.gov/pubmed/37126564 http://dx.doi.org/10.1126/sciadv.adf5143 |
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author | Wan Mohamad Noor, Wan Nurul Izzati Nguyen, Nhung Thi Hong Cheong, Theng Ho Chek, Min Fey Hakoshima, Toshio Inaba, Takehiko Hanawa-Suetsugu, Kyoko Nishimura, Tamako Suetsugu, Shiro |
author_facet | Wan Mohamad Noor, Wan Nurul Izzati Nguyen, Nhung Thi Hong Cheong, Theng Ho Chek, Min Fey Hakoshima, Toshio Inaba, Takehiko Hanawa-Suetsugu, Kyoko Nishimura, Tamako Suetsugu, Shiro |
author_sort | Wan Mohamad Noor, Wan Nurul Izzati |
collection | PubMed |
description | The higher-order assembly of Bin-amphiphysin-Rvs (BAR) domain proteins, including the FCH-BAR (F-BAR) domain proteins, into lattice on the membrane is essential for the formation of subcellular structures. However, the regulation of their ordered assembly has not been elucidated. Here, we show that the higher ordered assembly of growth-arrested specific 7 (GAS7), an F-BAR domain protein, is regulated by the multivalent scaffold proteins of Wiskott-Aldrich syndrome protein (WASP)/neural WASP, that commonly binds to the BAR domain superfamily proteins, together with WISH, Nck, the activated small guanosine triphosphatase Cdc42, and a membrane-anchored phagocytic receptor. The assembly kinetics by fluorescence resonance energy transfer monitoring indicated that the GAS7 assembly on liposomes started within seconds and was further increased by the presence of these proteins. The regulated GAS7 assembly was abolished by Wiskott-Aldrich syndrome mutations both in vitro and in cellular phagocytosis. Therefore, Cdc42 and the scaffold proteins that commonly bind to the BAR domain superfamily proteins promoted GAS7 assembly. |
format | Online Article Text |
id | pubmed-10132759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-101327592023-04-27 Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein Wan Mohamad Noor, Wan Nurul Izzati Nguyen, Nhung Thi Hong Cheong, Theng Ho Chek, Min Fey Hakoshima, Toshio Inaba, Takehiko Hanawa-Suetsugu, Kyoko Nishimura, Tamako Suetsugu, Shiro Sci Adv Biomedicine and Life Sciences The higher-order assembly of Bin-amphiphysin-Rvs (BAR) domain proteins, including the FCH-BAR (F-BAR) domain proteins, into lattice on the membrane is essential for the formation of subcellular structures. However, the regulation of their ordered assembly has not been elucidated. Here, we show that the higher ordered assembly of growth-arrested specific 7 (GAS7), an F-BAR domain protein, is regulated by the multivalent scaffold proteins of Wiskott-Aldrich syndrome protein (WASP)/neural WASP, that commonly binds to the BAR domain superfamily proteins, together with WISH, Nck, the activated small guanosine triphosphatase Cdc42, and a membrane-anchored phagocytic receptor. The assembly kinetics by fluorescence resonance energy transfer monitoring indicated that the GAS7 assembly on liposomes started within seconds and was further increased by the presence of these proteins. The regulated GAS7 assembly was abolished by Wiskott-Aldrich syndrome mutations both in vitro and in cellular phagocytosis. Therefore, Cdc42 and the scaffold proteins that commonly bind to the BAR domain superfamily proteins promoted GAS7 assembly. American Association for the Advancement of Science 2023-04-26 /pmc/articles/PMC10132759/ /pubmed/37126564 http://dx.doi.org/10.1126/sciadv.adf5143 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Wan Mohamad Noor, Wan Nurul Izzati Nguyen, Nhung Thi Hong Cheong, Theng Ho Chek, Min Fey Hakoshima, Toshio Inaba, Takehiko Hanawa-Suetsugu, Kyoko Nishimura, Tamako Suetsugu, Shiro Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein |
title | Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein |
title_full | Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein |
title_fullStr | Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein |
title_full_unstemmed | Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein |
title_short | Small GTPase Cdc42, WASP, and scaffold proteins for higher-order assembly of the F-BAR domain protein |
title_sort | small gtpase cdc42, wasp, and scaffold proteins for higher-order assembly of the f-bar domain protein |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132759/ https://www.ncbi.nlm.nih.gov/pubmed/37126564 http://dx.doi.org/10.1126/sciadv.adf5143 |
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