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Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin
Detailed knowledge on the formation of biomembrane domains, their structure, composition, and physical characteristics is scarce. Despite its frequently discussed importance in signaling, e.g., in obtaining localized non-homogeneous receptor compositions in the plasma membrane, the nanometer size as...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734319/ https://www.ncbi.nlm.nih.gov/pubmed/33330494 http://dx.doi.org/10.3389/fcell.2020.601145 |
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author | Bochicchio, Anna Brandner, Astrid F. Engberg, Oskar Huster, Daniel Böckmann, Rainer A. |
author_facet | Bochicchio, Anna Brandner, Astrid F. Engberg, Oskar Huster, Daniel Böckmann, Rainer A. |
author_sort | Bochicchio, Anna |
collection | PubMed |
description | Detailed knowledge on the formation of biomembrane domains, their structure, composition, and physical characteristics is scarce. Despite its frequently discussed importance in signaling, e.g., in obtaining localized non-homogeneous receptor compositions in the plasma membrane, the nanometer size as well as the dynamic and transient nature of domains impede their experimental characterization. In turn, atomistic molecular dynamics (MD) simulations combine both, high spatial and high temporal resolution. Here, using microsecond atomistic MD simulations, we characterize the spontaneous and unbiased formation of nano-domains in a plasma membrane model containing phosphatidylcholine (POPC), palmitoyl-sphingomyelin (PSM), and cholesterol (Chol) in the presence or absence of the neurotransmitter serotonin at different temperatures. In the ternary mixture, highly ordered and highly disordered domains of similar composition coexist at 303 K. The distinction of domains by lipid acyl chain order gets lost at lower temperatures of 298 and 294 K, suggesting a phase transition at ambient temperature. By comparison of domain ordering and composition, we demonstrate how the domain-specific binding of the neurotransmitter serotonin results in a modified domain lipid composition and a substantial downward shift of the phase transition temperature. Our simulations thus suggest a novel mode of action of neurotransmitters possibly of importance in neuronal signal transmission. |
format | Online Article Text |
id | pubmed-7734319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77343192020-12-15 Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin Bochicchio, Anna Brandner, Astrid F. Engberg, Oskar Huster, Daniel Böckmann, Rainer A. Front Cell Dev Biol Cell and Developmental Biology Detailed knowledge on the formation of biomembrane domains, their structure, composition, and physical characteristics is scarce. Despite its frequently discussed importance in signaling, e.g., in obtaining localized non-homogeneous receptor compositions in the plasma membrane, the nanometer size as well as the dynamic and transient nature of domains impede their experimental characterization. In turn, atomistic molecular dynamics (MD) simulations combine both, high spatial and high temporal resolution. Here, using microsecond atomistic MD simulations, we characterize the spontaneous and unbiased formation of nano-domains in a plasma membrane model containing phosphatidylcholine (POPC), palmitoyl-sphingomyelin (PSM), and cholesterol (Chol) in the presence or absence of the neurotransmitter serotonin at different temperatures. In the ternary mixture, highly ordered and highly disordered domains of similar composition coexist at 303 K. The distinction of domains by lipid acyl chain order gets lost at lower temperatures of 298 and 294 K, suggesting a phase transition at ambient temperature. By comparison of domain ordering and composition, we demonstrate how the domain-specific binding of the neurotransmitter serotonin results in a modified domain lipid composition and a substantial downward shift of the phase transition temperature. Our simulations thus suggest a novel mode of action of neurotransmitters possibly of importance in neuronal signal transmission. Frontiers Media S.A. 2020-11-30 /pmc/articles/PMC7734319/ /pubmed/33330494 http://dx.doi.org/10.3389/fcell.2020.601145 Text en Copyright © 2020 Bochicchio, Brandner, Engberg, Huster and Böckmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Bochicchio, Anna Brandner, Astrid F. Engberg, Oskar Huster, Daniel Böckmann, Rainer A. Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin |
title | Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin |
title_full | Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin |
title_fullStr | Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin |
title_full_unstemmed | Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin |
title_short | Spontaneous Membrane Nanodomain Formation in the Absence or Presence of the Neurotransmitter Serotonin |
title_sort | spontaneous membrane nanodomain formation in the absence or presence of the neurotransmitter serotonin |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734319/ https://www.ncbi.nlm.nih.gov/pubmed/33330494 http://dx.doi.org/10.3389/fcell.2020.601145 |
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