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Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid

Cellular membranes are composed of thousands of different lipids usually maintained within a narrow range of concentrations. In addition to their well-known structural and metabolic roles, signaling functions for many lipids have also emerged over the last two decades. The latter largely depend on t...

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Detalles Bibliográficos
Autores principales: Tanguy, Emeline, Kassas, Nawal, Vitale, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022864/
https://www.ncbi.nlm.nih.gov/pubmed/29690573
http://dx.doi.org/10.3390/biom8020020
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author Tanguy, Emeline
Kassas, Nawal
Vitale, Nicolas
author_facet Tanguy, Emeline
Kassas, Nawal
Vitale, Nicolas
author_sort Tanguy, Emeline
collection PubMed
description Cellular membranes are composed of thousands of different lipids usually maintained within a narrow range of concentrations. In addition to their well-known structural and metabolic roles, signaling functions for many lipids have also emerged over the last two decades. The latter largely depend on the ability of particular classes of lipids to interact specifically with a great variety of proteins and to regulate their localization and activity. Among these lipids, phosphatidic acid (PA) plays a unique role in a large repertoire of cellular activities, most likely in relation to its unique biophysical properties. However, until recently, only incomplete information was available to model the interaction between PA and its protein partners. The development of new liposome-based assays as well as molecular dynamic simulation are now providing novel information. We will review the different factors that have shown to modulate the capacity of PA to interact with specific domains in target proteins.
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spelling pubmed-60228642018-07-02 Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid Tanguy, Emeline Kassas, Nawal Vitale, Nicolas Biomolecules Review Cellular membranes are composed of thousands of different lipids usually maintained within a narrow range of concentrations. In addition to their well-known structural and metabolic roles, signaling functions for many lipids have also emerged over the last two decades. The latter largely depend on the ability of particular classes of lipids to interact specifically with a great variety of proteins and to regulate their localization and activity. Among these lipids, phosphatidic acid (PA) plays a unique role in a large repertoire of cellular activities, most likely in relation to its unique biophysical properties. However, until recently, only incomplete information was available to model the interaction between PA and its protein partners. The development of new liposome-based assays as well as molecular dynamic simulation are now providing novel information. We will review the different factors that have shown to modulate the capacity of PA to interact with specific domains in target proteins. MDPI 2018-04-23 /pmc/articles/PMC6022864/ /pubmed/29690573 http://dx.doi.org/10.3390/biom8020020 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tanguy, Emeline
Kassas, Nawal
Vitale, Nicolas
Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid
title Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid
title_full Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid
title_fullStr Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid
title_full_unstemmed Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid
title_short Protein–Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid
title_sort protein–phospholipid interaction motifs: a focus on phosphatidic acid
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022864/
https://www.ncbi.nlm.nih.gov/pubmed/29690573
http://dx.doi.org/10.3390/biom8020020
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