Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions
[Display omitted] Protein body (PB) formation in wheat seeds is a critical process influencing seed content and nutritional quality. In this study, we investigate the potential mechanisms governing PB formation through an in vitro approach, focusing on γ-gliadin, a key wheat storage protein. We used...
Gespeichert in:
Veröffentlicht in: | Journal of colloid and interface science 2024-08, Vol.668, p.252-263 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 263 |
---|---|
container_issue | |
container_start_page | 252 |
container_title | Journal of colloid and interface science |
container_volume | 668 |
creator | Cochereau, Rémy Voisin, Hugo Solé-Jamault, Véronique Novales, Bruno Davy, Joëlle Jamme, Frédéric Renard, Denis Boire, Adeline |
description | [Display omitted]
Protein body (PB) formation in wheat seeds is a critical process influencing seed content and nutritional quality. In this study, we investigate the potential mechanisms governing PB formation through an in vitro approach, focusing on γ-gliadin, a key wheat storage protein. We used a microfluidic technique to encapsulate γ-gliadin within giant unilamellar vesicles (GUVs) and tune the physicochemical conditions in a controlled and rapid way. We examined the influence of pH and protein concentration on LLPS and protein-membrane interactions using various microscopy and spectroscopy techniques. We showed that γ-gliadin encapsulated in GUVs can undergo a pH-triggered liquid–liquid phase separation (LLPS) by two distinct mechanisms depending on the γ-gliadin concentration. At low protein concentrations, γ-gliadins phase separate by a nucleation and growth-like process, while, at higher protein concentration and pH above 6.0, γ-gliadin formed a bi-continuous phase suggesting a spinodal decomposition-like mechanism. Fluorescence and microscopy data suggested that γ-gliadin dense phase exhibited affinity for the GUV membrane, forming a layer at the interface and affecting the reversibility of the phase separation. |
doi_str_mv | 10.1016/j.jcis.2024.04.136 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04680271v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021979724008646</els_id><sourcerecordid>3048497438</sourcerecordid><originalsourceid>FETCH-LOGICAL-c385t-4ad15d12ebf11f104448dad52ac3ccad9c9dbb14be6af73c2c620453bb5bdc923</originalsourceid><addsrcrecordid>eNp9kUtq3TAUhkVoSG7SbqCDomE7sKMjybYMnYTQ5gYuZNKOhV7u1cWvSHZKZ91Dl5J9ZBFdSWScZBgQSBx9-nU4H0IfgeRAoLw45AfjY04J5TnhObDyCG2A1EVWAWHv0IYQClld1dUpOovxQAhAUdQn6JSJshJCwAZNN33Tzq43Dg8NHrdY9Ra3fvQWd67TQfXposfT3qXq3ezt_7__1gMe9yo6HN2ogpp8glLA771TE358yH61Xlnf47TU3eyGOWIz9NYvYHyPjhvVRvfheT9HP79_-3G1zXa31zdXl7vMMFFMGVcWCgvU6QagAcI5F1bZgirDjFG2NrXVGrh2pWoqZqgpKeEF07rQ1tSUnaMva-5etXIMvlPhjxyUl9vLnVxqhJeC0AruIbGfV3YMQ2o4TrLz0bi2TRNI3UtGuOB1xZlIKF1RE4YYg2tes4HIxYw8yMWMXMykP2Qykx59es6fdefs65MXFQn4ugIuTeTeuyCj8YsY64Mzk7SDfyv_Cc2Eomg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3048497438</pqid></control><display><type>article</type><title>Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Cochereau, Rémy ; Voisin, Hugo ; Solé-Jamault, Véronique ; Novales, Bruno ; Davy, Joëlle ; Jamme, Frédéric ; Renard, Denis ; Boire, Adeline</creator><creatorcontrib>Cochereau, Rémy ; Voisin, Hugo ; Solé-Jamault, Véronique ; Novales, Bruno ; Davy, Joëlle ; Jamme, Frédéric ; Renard, Denis ; Boire, Adeline</creatorcontrib><description>[Display omitted]
Protein body (PB) formation in wheat seeds is a critical process influencing seed content and nutritional quality. In this study, we investigate the potential mechanisms governing PB formation through an in vitro approach, focusing on γ-gliadin, a key wheat storage protein. We used a microfluidic technique to encapsulate γ-gliadin within giant unilamellar vesicles (GUVs) and tune the physicochemical conditions in a controlled and rapid way. We examined the influence of pH and protein concentration on LLPS and protein-membrane interactions using various microscopy and spectroscopy techniques. We showed that γ-gliadin encapsulated in GUVs can undergo a pH-triggered liquid–liquid phase separation (LLPS) by two distinct mechanisms depending on the γ-gliadin concentration. At low protein concentrations, γ-gliadins phase separate by a nucleation and growth-like process, while, at higher protein concentration and pH above 6.0, γ-gliadin formed a bi-continuous phase suggesting a spinodal decomposition-like mechanism. Fluorescence and microscopy data suggested that γ-gliadin dense phase exhibited affinity for the GUV membrane, forming a layer at the interface and affecting the reversibility of the phase separation.</description><identifier>ISSN: 0021-9797</identifier><identifier>ISSN: 1095-7103</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2024.04.136</identifier><identifier>PMID: 38678881</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Food engineering ; Gliadin - chemistry ; Gliadin - isolation & purification ; Hydrogen-Ion Concentration ; Life Sciences ; Membrane Lipids - chemistry ; Phase Separation ; Triticum - chemistry ; Unilamellar Liposomes - chemistry ; Unilamellar Liposomes - metabolism ; Water - chemistry</subject><ispartof>Journal of colloid and interface science, 2024-08, Vol.668, p.252-263</ispartof><rights>2024 The Author(s)</rights><rights>Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><rights>Attribution - NonCommercial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c385t-4ad15d12ebf11f104448dad52ac3ccad9c9dbb14be6af73c2c620453bb5bdc923</cites><orcidid>0000-0002-6221-7630 ; 0000-0002-7897-3617 ; 0000-0002-0555-8826 ; 0000-0002-7398-7868 ; 0000-0001-9495-7660 ; 0000-0002-3515-0194</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021979724008646$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38678881$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-04680271$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Cochereau, Rémy</creatorcontrib><creatorcontrib>Voisin, Hugo</creatorcontrib><creatorcontrib>Solé-Jamault, Véronique</creatorcontrib><creatorcontrib>Novales, Bruno</creatorcontrib><creatorcontrib>Davy, Joëlle</creatorcontrib><creatorcontrib>Jamme, Frédéric</creatorcontrib><creatorcontrib>Renard, Denis</creatorcontrib><creatorcontrib>Boire, Adeline</creatorcontrib><title>Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>[Display omitted]
Protein body (PB) formation in wheat seeds is a critical process influencing seed content and nutritional quality. In this study, we investigate the potential mechanisms governing PB formation through an in vitro approach, focusing on γ-gliadin, a key wheat storage protein. We used a microfluidic technique to encapsulate γ-gliadin within giant unilamellar vesicles (GUVs) and tune the physicochemical conditions in a controlled and rapid way. We examined the influence of pH and protein concentration on LLPS and protein-membrane interactions using various microscopy and spectroscopy techniques. We showed that γ-gliadin encapsulated in GUVs can undergo a pH-triggered liquid–liquid phase separation (LLPS) by two distinct mechanisms depending on the γ-gliadin concentration. At low protein concentrations, γ-gliadins phase separate by a nucleation and growth-like process, while, at higher protein concentration and pH above 6.0, γ-gliadin formed a bi-continuous phase suggesting a spinodal decomposition-like mechanism. Fluorescence and microscopy data suggested that γ-gliadin dense phase exhibited affinity for the GUV membrane, forming a layer at the interface and affecting the reversibility of the phase separation.</description><subject>Food engineering</subject><subject>Gliadin - chemistry</subject><subject>Gliadin - isolation & purification</subject><subject>Hydrogen-Ion Concentration</subject><subject>Life Sciences</subject><subject>Membrane Lipids - chemistry</subject><subject>Phase Separation</subject><subject>Triticum - chemistry</subject><subject>Unilamellar Liposomes - chemistry</subject><subject>Unilamellar Liposomes - metabolism</subject><subject>Water - chemistry</subject><issn>0021-9797</issn><issn>1095-7103</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtq3TAUhkVoSG7SbqCDomE7sKMjybYMnYTQ5gYuZNKOhV7u1cWvSHZKZ91Dl5J9ZBFdSWScZBgQSBx9-nU4H0IfgeRAoLw45AfjY04J5TnhObDyCG2A1EVWAWHv0IYQClld1dUpOovxQAhAUdQn6JSJshJCwAZNN33Tzq43Dg8NHrdY9Ra3fvQWd67TQfXposfT3qXq3ezt_7__1gMe9yo6HN2ogpp8glLA771TE358yH61Xlnf47TU3eyGOWIz9NYvYHyPjhvVRvfheT9HP79_-3G1zXa31zdXl7vMMFFMGVcWCgvU6QagAcI5F1bZgirDjFG2NrXVGrh2pWoqZqgpKeEF07rQ1tSUnaMva-5etXIMvlPhjxyUl9vLnVxqhJeC0AruIbGfV3YMQ2o4TrLz0bi2TRNI3UtGuOB1xZlIKF1RE4YYg2tes4HIxYw8yMWMXMykP2Qykx59es6fdefs65MXFQn4ugIuTeTeuyCj8YsY64Mzk7SDfyv_Cc2Eomg</recordid><startdate>20240815</startdate><enddate>20240815</enddate><creator>Cochereau, Rémy</creator><creator>Voisin, Hugo</creator><creator>Solé-Jamault, Véronique</creator><creator>Novales, Bruno</creator><creator>Davy, Joëlle</creator><creator>Jamme, Frédéric</creator><creator>Renard, Denis</creator><creator>Boire, Adeline</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-6221-7630</orcidid><orcidid>https://orcid.org/0000-0002-7897-3617</orcidid><orcidid>https://orcid.org/0000-0002-0555-8826</orcidid><orcidid>https://orcid.org/0000-0002-7398-7868</orcidid><orcidid>https://orcid.org/0000-0001-9495-7660</orcidid><orcidid>https://orcid.org/0000-0002-3515-0194</orcidid></search><sort><creationdate>20240815</creationdate><title>Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions</title><author>Cochereau, Rémy ; Voisin, Hugo ; Solé-Jamault, Véronique ; Novales, Bruno ; Davy, Joëlle ; Jamme, Frédéric ; Renard, Denis ; Boire, Adeline</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-4ad15d12ebf11f104448dad52ac3ccad9c9dbb14be6af73c2c620453bb5bdc923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Food engineering</topic><topic>Gliadin - chemistry</topic><topic>Gliadin - isolation & purification</topic><topic>Hydrogen-Ion Concentration</topic><topic>Life Sciences</topic><topic>Membrane Lipids - chemistry</topic><topic>Phase Separation</topic><topic>Triticum - chemistry</topic><topic>Unilamellar Liposomes - chemistry</topic><topic>Unilamellar Liposomes - metabolism</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cochereau, Rémy</creatorcontrib><creatorcontrib>Voisin, Hugo</creatorcontrib><creatorcontrib>Solé-Jamault, Véronique</creatorcontrib><creatorcontrib>Novales, Bruno</creatorcontrib><creatorcontrib>Davy, Joëlle</creatorcontrib><creatorcontrib>Jamme, Frédéric</creatorcontrib><creatorcontrib>Renard, Denis</creatorcontrib><creatorcontrib>Boire, Adeline</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cochereau, Rémy</au><au>Voisin, Hugo</au><au>Solé-Jamault, Véronique</au><au>Novales, Bruno</au><au>Davy, Joëlle</au><au>Jamme, Frédéric</au><au>Renard, Denis</au><au>Boire, Adeline</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2024-08-15</date><risdate>2024</risdate><volume>668</volume><spage>252</spage><epage>263</epage><pages>252-263</pages><issn>0021-9797</issn><issn>1095-7103</issn><eissn>1095-7103</eissn><abstract>[Display omitted]
Protein body (PB) formation in wheat seeds is a critical process influencing seed content and nutritional quality. In this study, we investigate the potential mechanisms governing PB formation through an in vitro approach, focusing on γ-gliadin, a key wheat storage protein. We used a microfluidic technique to encapsulate γ-gliadin within giant unilamellar vesicles (GUVs) and tune the physicochemical conditions in a controlled and rapid way. We examined the influence of pH and protein concentration on LLPS and protein-membrane interactions using various microscopy and spectroscopy techniques. We showed that γ-gliadin encapsulated in GUVs can undergo a pH-triggered liquid–liquid phase separation (LLPS) by two distinct mechanisms depending on the γ-gliadin concentration. At low protein concentrations, γ-gliadins phase separate by a nucleation and growth-like process, while, at higher protein concentration and pH above 6.0, γ-gliadin formed a bi-continuous phase suggesting a spinodal decomposition-like mechanism. Fluorescence and microscopy data suggested that γ-gliadin dense phase exhibited affinity for the GUV membrane, forming a layer at the interface and affecting the reversibility of the phase separation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38678881</pmid><doi>10.1016/j.jcis.2024.04.136</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-6221-7630</orcidid><orcidid>https://orcid.org/0000-0002-7897-3617</orcidid><orcidid>https://orcid.org/0000-0002-0555-8826</orcidid><orcidid>https://orcid.org/0000-0002-7398-7868</orcidid><orcidid>https://orcid.org/0000-0001-9495-7660</orcidid><orcidid>https://orcid.org/0000-0002-3515-0194</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9797 |
ispartof | Journal of colloid and interface science, 2024-08, Vol.668, p.252-263 |
issn | 0021-9797 1095-7103 1095-7103 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_04680271v1 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Food engineering Gliadin - chemistry Gliadin - isolation & purification Hydrogen-Ion Concentration Life Sciences Membrane Lipids - chemistry Phase Separation Triticum - chemistry Unilamellar Liposomes - chemistry Unilamellar Liposomes - metabolism Water - chemistry |
title | Influence of pH and lipid membrane on the liquid–liquid phase separation of wheat γ-gliadin in aqueous conditions |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T00%3A16%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Influence%20of%20pH%20and%20lipid%20membrane%20on%20the%20liquid%E2%80%93liquid%20phase%20separation%20of%20wheat%20%CE%B3-gliadin%20in%20aqueous%20conditions&rft.jtitle=Journal%20of%20colloid%20and%20interface%20science&rft.au=Cochereau,%20R%C3%A9my&rft.date=2024-08-15&rft.volume=668&rft.spage=252&rft.epage=263&rft.pages=252-263&rft.issn=0021-9797&rft.eissn=1095-7103&rft_id=info:doi/10.1016/j.jcis.2024.04.136&rft_dat=%3Cproquest_hal_p%3E3048497438%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3048497438&rft_id=info:pmid/38678881&rft_els_id=S0021979724008646&rfr_iscdi=true |