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PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex
Protein S-acylation is a reversible post-translational modification involving the addition of fatty acids to cysteines and is catalyzed by transmembrane protein acyltransferases (PATs) mainly expressed at the Golgi complex. In case of soluble proteins, S-acylation confers stable membrane attachment....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944663/ https://www.ncbi.nlm.nih.gov/pubmed/31854448 http://dx.doi.org/10.1042/BSR20192911 |
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author | Chumpen Ramirez, Sabrina Astrada, Micaela R. Daniotti, Jose L. |
author_facet | Chumpen Ramirez, Sabrina Astrada, Micaela R. Daniotti, Jose L. |
author_sort | Chumpen Ramirez, Sabrina |
collection | PubMed |
description | Protein S-acylation is a reversible post-translational modification involving the addition of fatty acids to cysteines and is catalyzed by transmembrane protein acyltransferases (PATs) mainly expressed at the Golgi complex. In case of soluble proteins, S-acylation confers stable membrane attachment. Myristoylation or farnesylation of many soluble proteins constitutes the initial transient membrane adsorption step prior to S-acylation. However, some S-acylated soluble proteins, such as the neuronal growth-associated protein Growth-associated protein-43 (GAP-43), lack the hydrophobic modifications required for this initial membrane interaction. The signals for GAP-43 S-acylation are confined to the first 13 amino acids, including the S-acylatable cysteines 3 and 4 embedded in a hydrophobic region, followed by a cluster of basic amino acids. We found that mutation of critical basic amino acids drastically reduced membrane interaction and hence S-acylation of GAP-43. Interestingly, acute depletion of phosphatidylinositol 4-phosphate (PtdIns4P) at the Golgi complex reduced GAP-43 membrane binding, highlighting a new, pivotal role for this anionic lipid and supporting the idea that basic amino acid residues are involved in the electrostatic interactions between GAP-43 and membranes of the Golgi complex where they are S-acylated. |
format | Online Article Text |
id | pubmed-6944663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69446632020-01-09 PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex Chumpen Ramirez, Sabrina Astrada, Micaela R. Daniotti, Jose L. Biosci Rep Cell Membranes, Excitation & Transport Protein S-acylation is a reversible post-translational modification involving the addition of fatty acids to cysteines and is catalyzed by transmembrane protein acyltransferases (PATs) mainly expressed at the Golgi complex. In case of soluble proteins, S-acylation confers stable membrane attachment. Myristoylation or farnesylation of many soluble proteins constitutes the initial transient membrane adsorption step prior to S-acylation. However, some S-acylated soluble proteins, such as the neuronal growth-associated protein Growth-associated protein-43 (GAP-43), lack the hydrophobic modifications required for this initial membrane interaction. The signals for GAP-43 S-acylation are confined to the first 13 amino acids, including the S-acylatable cysteines 3 and 4 embedded in a hydrophobic region, followed by a cluster of basic amino acids. We found that mutation of critical basic amino acids drastically reduced membrane interaction and hence S-acylation of GAP-43. Interestingly, acute depletion of phosphatidylinositol 4-phosphate (PtdIns4P) at the Golgi complex reduced GAP-43 membrane binding, highlighting a new, pivotal role for this anionic lipid and supporting the idea that basic amino acid residues are involved in the electrostatic interactions between GAP-43 and membranes of the Golgi complex where they are S-acylated. Portland Press Ltd. 2020-01-06 /pmc/articles/PMC6944663/ /pubmed/31854448 http://dx.doi.org/10.1042/BSR20192911 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Cell Membranes, Excitation & Transport Chumpen Ramirez, Sabrina Astrada, Micaela R. Daniotti, Jose L. PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex |
title | PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex |
title_full | PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex |
title_fullStr | PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex |
title_full_unstemmed | PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex |
title_short | PtdIns4P-mediated electrostatic forces influence S-acylation of peripheral proteins at the Golgi complex |
title_sort | ptdins4p-mediated electrostatic forces influence s-acylation of peripheral proteins at the golgi complex |
topic | Cell Membranes, Excitation & Transport |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944663/ https://www.ncbi.nlm.nih.gov/pubmed/31854448 http://dx.doi.org/10.1042/BSR20192911 |
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