Differential targeting of membrane lipid domains by caffeic acid and its ester derivatives
Phenolic acids have been associated to a wide range of important health benefits underlain by a common molecular mechanism of action. Considering that significant membrane permeation is prevented by their hydrophilic character, we hypothesize that their main effects result from the interplay with ce...
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creator | Filipe, Hugo A.L. Sousa, Carla Marquês, Joaquim T. Vila-Viçosa, Diogo de Granada-Flor, António Viana, Ana S. Santos, M. Soledade C.S. Machuqueiro, Miguel de Almeida, Rodrigo F.M. |
description | Phenolic acids have been associated to a wide range of important health benefits underlain by a common molecular mechanism of action. Considering that significant membrane permeation is prevented by their hydrophilic character, we hypothesize that their main effects result from the interplay with cell membrane surface. This hypothesis was tested using the paradigmatic caffeic acid (CA) and two of its ester derivatives, rosmarinic (RA) and chlorogenic (CGA) acids, for which we predict, based on molecular dynamics simulations, a shallow location in phospholipid bilayers dependent on the protonation-state. Using complementary experimental approaches, an interaction with the membrane was definitely revealed for the three compounds, with RA exhibiting the highest lipid bilayer partition, and the redox signals of membrane-bound RA and CA being clearly detected. Cholesterol decreased the compounds bilayer partition, but not their ability to lower membrane dipole potential. In more complex membrane models containing also sphingomyelin, with liquid disordered (ld)/ liquid ordered (lo) phases coexistence, mimicking domains in the external leaflet of human plasma membrane, all compounds were able to affect nanodomains lateral organization. RA, and to a lesser extent CGA, decreased the size of lo domains. The most significant effect of CA was the possible formation of a rigid gel-like phase, enriched in sphingomyelin. In addition, all phenolic acids decreased the order of lo domains. In sum, phenolic acid effects on the membrane are enhanced in cholesterol-rich lo phases, which predominate in the outer leaflet of human cell membranes and are involved in many key cellular processes.
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•Phenolic acids interplay with membrane domains support diverse biological actions.•Lipid bilayer partition depends on phenolic acid structure and membrane cholesterol.•Redox signals of membrane-bound rosmarinic and caffeic acids were clearly detected.•Rosmarinic and chlorogenic acids disturb cholesterol-enriched domains.•Caffeic acid specifically targets sphingomyelin in membrane ordered domains. |
doi_str_mv | 10.1016/j.freeradbiomed.2017.12.002 |
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[Display omitted]
•Phenolic acids interplay with membrane domains support diverse biological actions.•Lipid bilayer partition depends on phenolic acid structure and membrane cholesterol.•Redox signals of membrane-bound rosmarinic and caffeic acids were clearly detected.•Rosmarinic and chlorogenic acids disturb cholesterol-enriched domains.•Caffeic acid specifically targets sphingomyelin in membrane ordered domains.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2017.12.002</identifier><identifier>PMID: 29221989</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antioxidant-membrane interactions ; Caffeic Acids - chemistry ; Caffeic Acids - metabolism ; Cell Membrane - metabolism ; Cells, Cultured ; Chlorogenic Acid - chemistry ; Chlorogenic Acid - metabolism ; Cholesterol - chemistry ; Cholesterol - metabolism ; Cinnamates - chemistry ; Cinnamates - metabolism ; Cyclic voltammetry ; Depsides - chemistry ; Depsides - metabolism ; Esters - chemistry ; Fluorescence spectroscopy ; Humans ; Hydroxybenzoates - chemistry ; Hydroxybenzoates - metabolism ; Hydroxycinnamic acids ; Lipid Bilayers - chemistry ; Lipid rafts ; Membrane Lipids - chemistry ; Membrane Lipids - metabolism ; Membrane Microdomains - metabolism ; Membrane model systems ; Membrane Potentials ; Molecular dynamics ; Molecular Dynamics Simulation ; Phospholipids ; Rosmarinic Acid ; Sphingomyelins - chemistry ; Sphingomyelins - metabolism</subject><ispartof>Free radical biology & medicine, 2018-02, Vol.115, p.232-245</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-57a3a706359c7db651a69865208ab914129bd1d9010bafc543071139a1dd62043</citedby><cites>FETCH-LOGICAL-c383t-57a3a706359c7db651a69865208ab914129bd1d9010bafc543071139a1dd62043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0891584917312340$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29221989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Filipe, Hugo A.L.</creatorcontrib><creatorcontrib>Sousa, Carla</creatorcontrib><creatorcontrib>Marquês, Joaquim T.</creatorcontrib><creatorcontrib>Vila-Viçosa, Diogo</creatorcontrib><creatorcontrib>de Granada-Flor, António</creatorcontrib><creatorcontrib>Viana, Ana S.</creatorcontrib><creatorcontrib>Santos, M. Soledade C.S.</creatorcontrib><creatorcontrib>Machuqueiro, Miguel</creatorcontrib><creatorcontrib>de Almeida, Rodrigo F.M.</creatorcontrib><title>Differential targeting of membrane lipid domains by caffeic acid and its ester derivatives</title><title>Free radical biology & medicine</title><addtitle>Free Radic Biol Med</addtitle><description>Phenolic acids have been associated to a wide range of important health benefits underlain by a common molecular mechanism of action. Considering that significant membrane permeation is prevented by their hydrophilic character, we hypothesize that their main effects result from the interplay with cell membrane surface. This hypothesis was tested using the paradigmatic caffeic acid (CA) and two of its ester derivatives, rosmarinic (RA) and chlorogenic (CGA) acids, for which we predict, based on molecular dynamics simulations, a shallow location in phospholipid bilayers dependent on the protonation-state. Using complementary experimental approaches, an interaction with the membrane was definitely revealed for the three compounds, with RA exhibiting the highest lipid bilayer partition, and the redox signals of membrane-bound RA and CA being clearly detected. Cholesterol decreased the compounds bilayer partition, but not their ability to lower membrane dipole potential. In more complex membrane models containing also sphingomyelin, with liquid disordered (ld)/ liquid ordered (lo) phases coexistence, mimicking domains in the external leaflet of human plasma membrane, all compounds were able to affect nanodomains lateral organization. RA, and to a lesser extent CGA, decreased the size of lo domains. The most significant effect of CA was the possible formation of a rigid gel-like phase, enriched in sphingomyelin. In addition, all phenolic acids decreased the order of lo domains. In sum, phenolic acid effects on the membrane are enhanced in cholesterol-rich lo phases, which predominate in the outer leaflet of human cell membranes and are involved in many key cellular processes.
[Display omitted]
•Phenolic acids interplay with membrane domains support diverse biological actions.•Lipid bilayer partition depends on phenolic acid structure and membrane cholesterol.•Redox signals of membrane-bound rosmarinic and caffeic acids were clearly detected.•Rosmarinic and chlorogenic acids disturb cholesterol-enriched domains.•Caffeic acid specifically targets sphingomyelin in membrane ordered domains.</description><subject>Antioxidant-membrane interactions</subject><subject>Caffeic Acids - chemistry</subject><subject>Caffeic Acids - metabolism</subject><subject>Cell Membrane - metabolism</subject><subject>Cells, Cultured</subject><subject>Chlorogenic Acid - chemistry</subject><subject>Chlorogenic Acid - metabolism</subject><subject>Cholesterol - chemistry</subject><subject>Cholesterol - metabolism</subject><subject>Cinnamates - chemistry</subject><subject>Cinnamates - metabolism</subject><subject>Cyclic voltammetry</subject><subject>Depsides - chemistry</subject><subject>Depsides - metabolism</subject><subject>Esters - chemistry</subject><subject>Fluorescence spectroscopy</subject><subject>Humans</subject><subject>Hydroxybenzoates - chemistry</subject><subject>Hydroxybenzoates - metabolism</subject><subject>Hydroxycinnamic acids</subject><subject>Lipid Bilayers - chemistry</subject><subject>Lipid rafts</subject><subject>Membrane Lipids - chemistry</subject><subject>Membrane Lipids - metabolism</subject><subject>Membrane Microdomains - metabolism</subject><subject>Membrane model systems</subject><subject>Membrane Potentials</subject><subject>Molecular dynamics</subject><subject>Molecular Dynamics Simulation</subject><subject>Phospholipids</subject><subject>Rosmarinic Acid</subject><subject>Sphingomyelins - chemistry</subject><subject>Sphingomyelins - metabolism</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE9vFDEMxSMEotvCV0CRuHCZaZxMZhJxQu1SkCr1AhcuUSbxVF7NnyWZXanfvllte-DGyZL9nv38Y-wziBoEtNe7ekiIyceelgljLQV0NchaCPmGbcB0qmq0bd-yjTAWKm0ae8Euc94JIRqtzHt2Ia2UYI3dsD-3NAyYcF7Jj3z16RFXmh_5MvAJpz75GflIe4o8LpOnOfP-iQdfPBS4D6Xv58hpzRzziolHTHT0Kx0xf2DvBj9m_PhSr9jv79tfNz-q-4e7nzff7qugjFor3XnlO9EqbUMX-1aDb61ptRTG9xYakLaPEK0A0fsh6EaJDkBZDzG2UjTqin05792n5e-hxHAT5YDjWLIvh-zAdlpIq4ws0q9naUhLzgkHt080-fTkQLgTXLdz_8B1J7gOpCtwi_vTy6FDf5q9el9pFsH2LMDy7pEwuRwI54CREobVxYX-69Az6a6SQw</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Filipe, Hugo A.L.</creator><creator>Sousa, Carla</creator><creator>Marquês, Joaquim T.</creator><creator>Vila-Viçosa, Diogo</creator><creator>de Granada-Flor, António</creator><creator>Viana, Ana S.</creator><creator>Santos, M. Soledade C.S.</creator><creator>Machuqueiro, Miguel</creator><creator>de Almeida, Rodrigo F.M.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180201</creationdate><title>Differential targeting of membrane lipid domains by caffeic acid and its ester derivatives</title><author>Filipe, Hugo A.L. ; Sousa, Carla ; Marquês, Joaquim T. ; Vila-Viçosa, Diogo ; de Granada-Flor, António ; Viana, Ana S. ; Santos, M. Soledade C.S. ; Machuqueiro, Miguel ; de Almeida, Rodrigo F.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-57a3a706359c7db651a69865208ab914129bd1d9010bafc543071139a1dd62043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antioxidant-membrane interactions</topic><topic>Caffeic Acids - chemistry</topic><topic>Caffeic Acids - metabolism</topic><topic>Cell Membrane - metabolism</topic><topic>Cells, Cultured</topic><topic>Chlorogenic Acid - chemistry</topic><topic>Chlorogenic Acid - metabolism</topic><topic>Cholesterol - chemistry</topic><topic>Cholesterol - metabolism</topic><topic>Cinnamates - chemistry</topic><topic>Cinnamates - metabolism</topic><topic>Cyclic voltammetry</topic><topic>Depsides - chemistry</topic><topic>Depsides - metabolism</topic><topic>Esters - chemistry</topic><topic>Fluorescence spectroscopy</topic><topic>Humans</topic><topic>Hydroxybenzoates - chemistry</topic><topic>Hydroxybenzoates - metabolism</topic><topic>Hydroxycinnamic acids</topic><topic>Lipid Bilayers - chemistry</topic><topic>Lipid rafts</topic><topic>Membrane Lipids - chemistry</topic><topic>Membrane Lipids - metabolism</topic><topic>Membrane Microdomains - metabolism</topic><topic>Membrane model systems</topic><topic>Membrane Potentials</topic><topic>Molecular dynamics</topic><topic>Molecular Dynamics Simulation</topic><topic>Phospholipids</topic><topic>Rosmarinic Acid</topic><topic>Sphingomyelins - chemistry</topic><topic>Sphingomyelins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Filipe, Hugo A.L.</creatorcontrib><creatorcontrib>Sousa, Carla</creatorcontrib><creatorcontrib>Marquês, Joaquim T.</creatorcontrib><creatorcontrib>Vila-Viçosa, Diogo</creatorcontrib><creatorcontrib>de Granada-Flor, António</creatorcontrib><creatorcontrib>Viana, Ana S.</creatorcontrib><creatorcontrib>Santos, M. Soledade C.S.</creatorcontrib><creatorcontrib>Machuqueiro, Miguel</creatorcontrib><creatorcontrib>de Almeida, Rodrigo F.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Free radical biology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Filipe, Hugo A.L.</au><au>Sousa, Carla</au><au>Marquês, Joaquim T.</au><au>Vila-Viçosa, Diogo</au><au>de Granada-Flor, António</au><au>Viana, Ana S.</au><au>Santos, M. Soledade C.S.</au><au>Machuqueiro, Miguel</au><au>de Almeida, Rodrigo F.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential targeting of membrane lipid domains by caffeic acid and its ester derivatives</atitle><jtitle>Free radical biology & medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2018-02-01</date><risdate>2018</risdate><volume>115</volume><spage>232</spage><epage>245</epage><pages>232-245</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>Phenolic acids have been associated to a wide range of important health benefits underlain by a common molecular mechanism of action. Considering that significant membrane permeation is prevented by their hydrophilic character, we hypothesize that their main effects result from the interplay with cell membrane surface. This hypothesis was tested using the paradigmatic caffeic acid (CA) and two of its ester derivatives, rosmarinic (RA) and chlorogenic (CGA) acids, for which we predict, based on molecular dynamics simulations, a shallow location in phospholipid bilayers dependent on the protonation-state. Using complementary experimental approaches, an interaction with the membrane was definitely revealed for the three compounds, with RA exhibiting the highest lipid bilayer partition, and the redox signals of membrane-bound RA and CA being clearly detected. Cholesterol decreased the compounds bilayer partition, but not their ability to lower membrane dipole potential. In more complex membrane models containing also sphingomyelin, with liquid disordered (ld)/ liquid ordered (lo) phases coexistence, mimicking domains in the external leaflet of human plasma membrane, all compounds were able to affect nanodomains lateral organization. RA, and to a lesser extent CGA, decreased the size of lo domains. The most significant effect of CA was the possible formation of a rigid gel-like phase, enriched in sphingomyelin. In addition, all phenolic acids decreased the order of lo domains. In sum, phenolic acid effects on the membrane are enhanced in cholesterol-rich lo phases, which predominate in the outer leaflet of human cell membranes and are involved in many key cellular processes.
[Display omitted]
•Phenolic acids interplay with membrane domains support diverse biological actions.•Lipid bilayer partition depends on phenolic acid structure and membrane cholesterol.•Redox signals of membrane-bound rosmarinic and caffeic acids were clearly detected.•Rosmarinic and chlorogenic acids disturb cholesterol-enriched domains.•Caffeic acid specifically targets sphingomyelin in membrane ordered domains.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29221989</pmid><doi>10.1016/j.freeradbiomed.2017.12.002</doi><tpages>14</tpages></addata></record> |
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subjects | Antioxidant-membrane interactions Caffeic Acids - chemistry Caffeic Acids - metabolism Cell Membrane - metabolism Cells, Cultured Chlorogenic Acid - chemistry Chlorogenic Acid - metabolism Cholesterol - chemistry Cholesterol - metabolism Cinnamates - chemistry Cinnamates - metabolism Cyclic voltammetry Depsides - chemistry Depsides - metabolism Esters - chemistry Fluorescence spectroscopy Humans Hydroxybenzoates - chemistry Hydroxybenzoates - metabolism Hydroxycinnamic acids Lipid Bilayers - chemistry Lipid rafts Membrane Lipids - chemistry Membrane Lipids - metabolism Membrane Microdomains - metabolism Membrane model systems Membrane Potentials Molecular dynamics Molecular Dynamics Simulation Phospholipids Rosmarinic Acid Sphingomyelins - chemistry Sphingomyelins - metabolism |
title | Differential targeting of membrane lipid domains by caffeic acid and its ester derivatives |
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