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Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein
Phosphatidylinositol 4-kinase beta (PI4KB) is one of four human PI4K enzymes that generate phosphatidylinositol 4-phosphate (PI4P), a minor but essential regulatory lipid found in all eukaryotic cells. To convert their lipid substrates, PI4Ks must be recruited to the correct membrane compartment. PI...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4806292/ https://www.ncbi.nlm.nih.gov/pubmed/27009356 http://dx.doi.org/10.1038/srep23641 |
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author | Klima, Martin Tóth, Dániel J. Hexnerova, Rozalie Baumlova, Adriana Chalupska, Dominika Tykvart, Jan Rezabkova, Lenka Sengupta, Nivedita Man, Petr Dubankova, Anna Humpolickova, Jana Nencka, Radim Veverka, Vaclav Balla, Tamas Boura, Evzen |
author_facet | Klima, Martin Tóth, Dániel J. Hexnerova, Rozalie Baumlova, Adriana Chalupska, Dominika Tykvart, Jan Rezabkova, Lenka Sengupta, Nivedita Man, Petr Dubankova, Anna Humpolickova, Jana Nencka, Radim Veverka, Vaclav Balla, Tamas Boura, Evzen |
author_sort | Klima, Martin |
collection | PubMed |
description | Phosphatidylinositol 4-kinase beta (PI4KB) is one of four human PI4K enzymes that generate phosphatidylinositol 4-phosphate (PI4P), a minor but essential regulatory lipid found in all eukaryotic cells. To convert their lipid substrates, PI4Ks must be recruited to the correct membrane compartment. PI4KB is critical for the maintenance of the Golgi and trans Golgi network (TGN) PI4P pools, however, the actual targeting mechanism of PI4KB to the Golgi and TGN membranes is unknown. Here, we present an NMR structure of the complex of PI4KB and its interacting partner, Golgi adaptor protein acyl-coenzyme A binding domain containing protein 3 (ACBD3). We show that ACBD3 is capable of recruiting PI4KB to membranes both in vitro and in vivo, and that membrane recruitment of PI4KB by ACBD3 increases its enzymatic activity and that the ACBD3:PI4KB complex formation is essential for proper function of the Golgi. |
format | Online Article Text |
id | pubmed-4806292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48062922016-03-24 Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein Klima, Martin Tóth, Dániel J. Hexnerova, Rozalie Baumlova, Adriana Chalupska, Dominika Tykvart, Jan Rezabkova, Lenka Sengupta, Nivedita Man, Petr Dubankova, Anna Humpolickova, Jana Nencka, Radim Veverka, Vaclav Balla, Tamas Boura, Evzen Sci Rep Article Phosphatidylinositol 4-kinase beta (PI4KB) is one of four human PI4K enzymes that generate phosphatidylinositol 4-phosphate (PI4P), a minor but essential regulatory lipid found in all eukaryotic cells. To convert their lipid substrates, PI4Ks must be recruited to the correct membrane compartment. PI4KB is critical for the maintenance of the Golgi and trans Golgi network (TGN) PI4P pools, however, the actual targeting mechanism of PI4KB to the Golgi and TGN membranes is unknown. Here, we present an NMR structure of the complex of PI4KB and its interacting partner, Golgi adaptor protein acyl-coenzyme A binding domain containing protein 3 (ACBD3). We show that ACBD3 is capable of recruiting PI4KB to membranes both in vitro and in vivo, and that membrane recruitment of PI4KB by ACBD3 increases its enzymatic activity and that the ACBD3:PI4KB complex formation is essential for proper function of the Golgi. Nature Publishing Group 2016-03-24 /pmc/articles/PMC4806292/ /pubmed/27009356 http://dx.doi.org/10.1038/srep23641 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Klima, Martin Tóth, Dániel J. Hexnerova, Rozalie Baumlova, Adriana Chalupska, Dominika Tykvart, Jan Rezabkova, Lenka Sengupta, Nivedita Man, Petr Dubankova, Anna Humpolickova, Jana Nencka, Radim Veverka, Vaclav Balla, Tamas Boura, Evzen Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein |
title | Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein |
title_full | Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein |
title_fullStr | Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein |
title_full_unstemmed | Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein |
title_short | Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein |
title_sort | structural insights and in vitro reconstitution of membrane targeting and activation of human pi4kb by the acbd3 protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4806292/ https://www.ncbi.nlm.nih.gov/pubmed/27009356 http://dx.doi.org/10.1038/srep23641 |
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