Preparation of supported lipid membranes for aquaporin Z incorporation
[Display omitted] ► Aquaporin Z (AqpZ) proteins were successfully incorporated into DOPC liposomes. ► Supported lipid membranes were prepared on NF membrane surface for AqpZ embedding. ► Spin coating plus vesicle fusion can make lipid membrane with low defect density. ► Inhibition of AqpZ function m...
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Veröffentlicht in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2012-06, Vol.94, p.333-340 |
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creator | Li, Xuesong Wang, Rong Tang, Chuyang Vararattanavech, Ardcharaporn Zhao, Yang Torres, Jaume Fane, Tony |
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► Aquaporin Z (AqpZ) proteins were successfully incorporated into DOPC liposomes. ► Supported lipid membranes were prepared on NF membrane surface for AqpZ embedding. ► Spin coating plus vesicle fusion can make lipid membrane with low defect density. ► Inhibition of AqpZ function may be caused by low lipid mobility on support surface.
There has been a recent surge of interest to mimic the performance of natural cellular membranes by incorporating water channel proteins-aquaporins (AQPs) into various ultrathin films for water filtration applications. To make biomimetic membranes one of the most crucial steps is preparing a defect-free platform for AQPs incorporation on a suitable substrate. In this study two methods were used to prepare supported lipid membranes on NF membrane surfaces under a benign pH condition of 7.8. One method was direct vesicle fusion on a hydrophilic membrane NF-270; the other was vesicle fusion facilitated by hydraulic pressure on a modified hydrophilic NF-270 membrane whose surface has been spin-coated with positively charged lipids.
Experiments revealed that the supported lipid membrane without AQPs prepared by the spin coating plus vesicle fusion had a much lower defect density than that prepared by vesicle fusion alone. It appears that the surface roughness and charge are the main factors determining the quality of the supported lipid membrane. Aquaporin Z (AqpZ) proteins were successfully incorporated into 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes and its permeability was measured by the stopped-flow experimental procedure. However, after the proteoliposomes have been fused onto the modified substrate, the AqpZ function in the resultant membrane was not observed and AFM images showed distinct aggregations of unfused proteoliposomes or AqpZ proteins on the substrate surface. It is speculated that the inhibition of AqpZ function may be caused by the low lipid mobility on the NF membrane surface. Further investigations to evaluate and optimize the structure-performance relationship are required. |
doi_str_mv | 10.1016/j.colsurfb.2012.02.013 |
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► Aquaporin Z (AqpZ) proteins were successfully incorporated into DOPC liposomes. ► Supported lipid membranes were prepared on NF membrane surface for AqpZ embedding. ► Spin coating plus vesicle fusion can make lipid membrane with low defect density. ► Inhibition of AqpZ function may be caused by low lipid mobility on support surface.
There has been a recent surge of interest to mimic the performance of natural cellular membranes by incorporating water channel proteins-aquaporins (AQPs) into various ultrathin films for water filtration applications. To make biomimetic membranes one of the most crucial steps is preparing a defect-free platform for AQPs incorporation on a suitable substrate. In this study two methods were used to prepare supported lipid membranes on NF membrane surfaces under a benign pH condition of 7.8. One method was direct vesicle fusion on a hydrophilic membrane NF-270; the other was vesicle fusion facilitated by hydraulic pressure on a modified hydrophilic NF-270 membrane whose surface has been spin-coated with positively charged lipids.
Experiments revealed that the supported lipid membrane without AQPs prepared by the spin coating plus vesicle fusion had a much lower defect density than that prepared by vesicle fusion alone. It appears that the surface roughness and charge are the main factors determining the quality of the supported lipid membrane. Aquaporin Z (AqpZ) proteins were successfully incorporated into 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes and its permeability was measured by the stopped-flow experimental procedure. However, after the proteoliposomes have been fused onto the modified substrate, the AqpZ function in the resultant membrane was not observed and AFM images showed distinct aggregations of unfused proteoliposomes or AqpZ proteins on the substrate surface. It is speculated that the inhibition of AqpZ function may be caused by the low lipid mobility on the NF membrane surface. Further investigations to evaluate and optimize the structure-performance relationship are required.</description><identifier>ISSN: 0927-7765</identifier><identifier>EISSN: 1873-4367</identifier><identifier>DOI: 10.1016/j.colsurfb.2012.02.013</identifier><identifier>PMID: 22386862</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Aquaporin Z ; aquaporins ; Aquaporins - chemistry ; artificial membranes ; Biomimetic Materials - chemical synthesis ; cell membranes ; coatings ; colloids ; Escherichia coli Proteins - chemistry ; Filtration ; Hydrogen-Ion Concentration ; hydrophilicity ; lipids ; Membrane Fusion ; Microscopy, Atomic Force ; NF-270 membrane ; Permeability ; Phosphatidylcholines - chemistry ; Proteolipids - chemistry ; Static Electricity ; Supported lipid membrane ; Surface Properties ; surface roughness ; Vesicle fusion ; Water Purification</subject><ispartof>Colloids and surfaces, B, Biointerfaces, 2012-06, Vol.94, p.333-340</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-aae213b46c3eb1d962f0fe62e9683b68f6720a63f3f882b179bb23cdabf358053</citedby><cites>FETCH-LOGICAL-c457t-aae213b46c3eb1d962f0fe62e9683b68f6720a63f3f882b179bb23cdabf358053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0927776512001221$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22386862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xuesong</creatorcontrib><creatorcontrib>Wang, Rong</creatorcontrib><creatorcontrib>Tang, Chuyang</creatorcontrib><creatorcontrib>Vararattanavech, Ardcharaporn</creatorcontrib><creatorcontrib>Zhao, Yang</creatorcontrib><creatorcontrib>Torres, Jaume</creatorcontrib><creatorcontrib>Fane, Tony</creatorcontrib><title>Preparation of supported lipid membranes for aquaporin Z incorporation</title><title>Colloids and surfaces, B, Biointerfaces</title><addtitle>Colloids Surf B Biointerfaces</addtitle><description>[Display omitted]
► Aquaporin Z (AqpZ) proteins were successfully incorporated into DOPC liposomes. ► Supported lipid membranes were prepared on NF membrane surface for AqpZ embedding. ► Spin coating plus vesicle fusion can make lipid membrane with low defect density. ► Inhibition of AqpZ function may be caused by low lipid mobility on support surface.
There has been a recent surge of interest to mimic the performance of natural cellular membranes by incorporating water channel proteins-aquaporins (AQPs) into various ultrathin films for water filtration applications. To make biomimetic membranes one of the most crucial steps is preparing a defect-free platform for AQPs incorporation on a suitable substrate. In this study two methods were used to prepare supported lipid membranes on NF membrane surfaces under a benign pH condition of 7.8. One method was direct vesicle fusion on a hydrophilic membrane NF-270; the other was vesicle fusion facilitated by hydraulic pressure on a modified hydrophilic NF-270 membrane whose surface has been spin-coated with positively charged lipids.
Experiments revealed that the supported lipid membrane without AQPs prepared by the spin coating plus vesicle fusion had a much lower defect density than that prepared by vesicle fusion alone. It appears that the surface roughness and charge are the main factors determining the quality of the supported lipid membrane. Aquaporin Z (AqpZ) proteins were successfully incorporated into 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes and its permeability was measured by the stopped-flow experimental procedure. However, after the proteoliposomes have been fused onto the modified substrate, the AqpZ function in the resultant membrane was not observed and AFM images showed distinct aggregations of unfused proteoliposomes or AqpZ proteins on the substrate surface. It is speculated that the inhibition of AqpZ function may be caused by the low lipid mobility on the NF membrane surface. Further investigations to evaluate and optimize the structure-performance relationship are required.</description><subject>Aquaporin Z</subject><subject>aquaporins</subject><subject>Aquaporins - chemistry</subject><subject>artificial membranes</subject><subject>Biomimetic Materials - chemical synthesis</subject><subject>cell membranes</subject><subject>coatings</subject><subject>colloids</subject><subject>Escherichia coli Proteins - chemistry</subject><subject>Filtration</subject><subject>Hydrogen-Ion Concentration</subject><subject>hydrophilicity</subject><subject>lipids</subject><subject>Membrane Fusion</subject><subject>Microscopy, Atomic Force</subject><subject>NF-270 membrane</subject><subject>Permeability</subject><subject>Phosphatidylcholines - chemistry</subject><subject>Proteolipids - chemistry</subject><subject>Static Electricity</subject><subject>Supported lipid membrane</subject><subject>Surface Properties</subject><subject>surface roughness</subject><subject>Vesicle fusion</subject><subject>Water Purification</subject><issn>0927-7765</issn><issn>1873-4367</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtKxDAUhoMoznh5hbE7Vx1z6STpThFvICioGzchSU8kQ9vUpBV8ezOOuhUOhJDv_3P4EFoQvCSY8LP10oY2TdGZJcWELnEewnbQnEjByopxsYvmuKaiFIKvZuggpTXGmFZE7KMZpUxyyekcXT9GGHTUow99EVyRpmEIcYSmaP3gm6KDzkTdQypciIV-n3R-9n3xWvjehpgv39EjtOd0m-D45zxEL9dXz5e35f3Dzd3lxX1pq5UYS62BEmYqbhkY0tScOuyAU6i5ZIZLxwXFmjPHnJTUEFEbQ5lttHFsJfGKHaLTbe8Qw_sEaVSdTxbaNq8YpqRqziStRUUzybekjSGlCE4N0Xc6fiqC1UahWqtfhWqjUOE8hOXg4ueLyXTQ_MV-nWXgZAs4HZR-iz6pl6fcwLNfxrHcVJxvCcgqPjxElayH3kLjI9hRNcH_t8UXq9aP5A</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Li, Xuesong</creator><creator>Wang, Rong</creator><creator>Tang, Chuyang</creator><creator>Vararattanavech, Ardcharaporn</creator><creator>Zhao, Yang</creator><creator>Torres, Jaume</creator><creator>Fane, Tony</creator><general>Elsevier B.V</general><scope>FBQ</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></search><sort><creationdate>20120601</creationdate><title>Preparation of supported lipid membranes for aquaporin Z incorporation</title><author>Li, Xuesong ; Wang, Rong ; Tang, Chuyang ; Vararattanavech, Ardcharaporn ; Zhao, Yang ; Torres, Jaume ; Fane, Tony</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-aae213b46c3eb1d962f0fe62e9683b68f6720a63f3f882b179bb23cdabf358053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aquaporin Z</topic><topic>aquaporins</topic><topic>Aquaporins - chemistry</topic><topic>artificial membranes</topic><topic>Biomimetic Materials - chemical synthesis</topic><topic>cell membranes</topic><topic>coatings</topic><topic>colloids</topic><topic>Escherichia coli Proteins - chemistry</topic><topic>Filtration</topic><topic>Hydrogen-Ion Concentration</topic><topic>hydrophilicity</topic><topic>lipids</topic><topic>Membrane Fusion</topic><topic>Microscopy, Atomic Force</topic><topic>NF-270 membrane</topic><topic>Permeability</topic><topic>Phosphatidylcholines - chemistry</topic><topic>Proteolipids - chemistry</topic><topic>Static Electricity</topic><topic>Supported lipid membrane</topic><topic>Surface Properties</topic><topic>surface roughness</topic><topic>Vesicle fusion</topic><topic>Water Purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xuesong</creatorcontrib><creatorcontrib>Wang, Rong</creatorcontrib><creatorcontrib>Tang, Chuyang</creatorcontrib><creatorcontrib>Vararattanavech, Ardcharaporn</creatorcontrib><creatorcontrib>Zhao, Yang</creatorcontrib><creatorcontrib>Torres, Jaume</creatorcontrib><creatorcontrib>Fane, Tony</creatorcontrib><collection>AGRIS</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><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xuesong</au><au>Wang, Rong</au><au>Tang, Chuyang</au><au>Vararattanavech, Ardcharaporn</au><au>Zhao, Yang</au><au>Torres, Jaume</au><au>Fane, Tony</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of supported lipid membranes for aquaporin Z incorporation</atitle><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle><addtitle>Colloids Surf B Biointerfaces</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>94</volume><spage>333</spage><epage>340</epage><pages>333-340</pages><issn>0927-7765</issn><eissn>1873-4367</eissn><abstract>[Display omitted]
► Aquaporin Z (AqpZ) proteins were successfully incorporated into DOPC liposomes. ► Supported lipid membranes were prepared on NF membrane surface for AqpZ embedding. ► Spin coating plus vesicle fusion can make lipid membrane with low defect density. ► Inhibition of AqpZ function may be caused by low lipid mobility on support surface.
There has been a recent surge of interest to mimic the performance of natural cellular membranes by incorporating water channel proteins-aquaporins (AQPs) into various ultrathin films for water filtration applications. To make biomimetic membranes one of the most crucial steps is preparing a defect-free platform for AQPs incorporation on a suitable substrate. In this study two methods were used to prepare supported lipid membranes on NF membrane surfaces under a benign pH condition of 7.8. One method was direct vesicle fusion on a hydrophilic membrane NF-270; the other was vesicle fusion facilitated by hydraulic pressure on a modified hydrophilic NF-270 membrane whose surface has been spin-coated with positively charged lipids.
Experiments revealed that the supported lipid membrane without AQPs prepared by the spin coating plus vesicle fusion had a much lower defect density than that prepared by vesicle fusion alone. It appears that the surface roughness and charge are the main factors determining the quality of the supported lipid membrane. Aquaporin Z (AqpZ) proteins were successfully incorporated into 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes and its permeability was measured by the stopped-flow experimental procedure. However, after the proteoliposomes have been fused onto the modified substrate, the AqpZ function in the resultant membrane was not observed and AFM images showed distinct aggregations of unfused proteoliposomes or AqpZ proteins on the substrate surface. It is speculated that the inhibition of AqpZ function may be caused by the low lipid mobility on the NF membrane surface. Further investigations to evaluate and optimize the structure-performance relationship are required.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>22386862</pmid><doi>10.1016/j.colsurfb.2012.02.013</doi><tpages>8</tpages></addata></record> |
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subjects | Aquaporin Z aquaporins Aquaporins - chemistry artificial membranes Biomimetic Materials - chemical synthesis cell membranes coatings colloids Escherichia coli Proteins - chemistry Filtration Hydrogen-Ion Concentration hydrophilicity lipids Membrane Fusion Microscopy, Atomic Force NF-270 membrane Permeability Phosphatidylcholines - chemistry Proteolipids - chemistry Static Electricity Supported lipid membrane Surface Properties surface roughness Vesicle fusion Water Purification |
title | Preparation of supported lipid membranes for aquaporin Z incorporation |
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