Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
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
_version_ 1785031458111356928
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
work_keys_str_mv AT wanmohamadnoorwannurulizzati smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT nguyennhungthihong smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT cheongthengho smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT chekminfey smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT hakoshimatoshio smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT inabatakehiko smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT hanawasuetsugukyoko smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT nishimuratamako smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein
AT suetsugushiro smallgtpasecdc42waspandscaffoldproteinsforhigherorderassemblyofthefbardomainprotein