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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....

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Autores principales: Chumpen Ramirez, Sabrina, Astrada, Micaela R., Daniotti, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
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.
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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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