Blistering of Langmuir-Blodgett Bilayers Containing Anionic Phospholipids as Observed by Atomic Force Microscopy
Asymmetric bilayers of different phospholipid compositions have been prepared by the Langmuir-Blodgett (L-B) method, and imaged by atomic force microscopy (AFM). Such bilayers can function as a model for biological membranes. The first leaflet consisted of zwitterionic phospholipids phosphatidylchol...
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description | Asymmetric bilayers of different phospholipid compositions have been prepared by the Langmuir-Blodgett (L-B) method, and imaged by atomic force microscopy (AFM). Such bilayers can function as a model for biological membranes. The first leaflet consisted of zwitterionic phospholipids phosphatidylcholine (PC) or phosphatidylethanolamine (PE). The second leaflet consisted of the anionic phospholipid phosphatidylglycerol (PG), in either the condensed or liquid phase or, for comparison, of PC. Different bilayers showed different morphology. In all bilayers defects in the form of holes were present. In some bilayers with a first leaflet consisting of PC, polygonal line-shaped defects were observed, whereas when the first leaflet consisted of PE, mainly round defects were seen. Not only the shape, but also the amount of defects varied, depending on the condition and the composition of the second leaflet. In most of the PG-containing systems the defects were surrounded by elevations, which reversibly disappeared in the presence of divalent cations. This is the first time that such elevations have been observed on phospholipid bilayers. We propose that they are induced by phospholipid exchange between the two leaflets around the defects, leading to the presence of negatively charged phospholipids in the first leaflet. Because the substrate is also negatively charged, the bilayer around the edges is repelled and lifted up. Since it was found that the elevations are indeed detached from the substrate, we refer to this effect as bilayer blistering. |
doi_str_mv | 10.1016/S0006-3495(99)77015-3 |
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Such bilayers can function as a model for biological membranes. The first leaflet consisted of zwitterionic phospholipids phosphatidylcholine (PC) or phosphatidylethanolamine (PE). The second leaflet consisted of the anionic phospholipid phosphatidylglycerol (PG), in either the condensed or liquid phase or, for comparison, of PC. Different bilayers showed different morphology. In all bilayers defects in the form of holes were present. In some bilayers with a first leaflet consisting of PC, polygonal line-shaped defects were observed, whereas when the first leaflet consisted of PE, mainly round defects were seen. Not only the shape, but also the amount of defects varied, depending on the condition and the composition of the second leaflet. In most of the PG-containing systems the defects were surrounded by elevations, which reversibly disappeared in the presence of divalent cations. This is the first time that such elevations have been observed on phospholipid bilayers. We propose that they are induced by phospholipid exchange between the two leaflets around the defects, leading to the presence of negatively charged phospholipids in the first leaflet. Because the substrate is also negatively charged, the bilayer around the edges is repelled and lifted up. Since it was found that the elevations are indeed detached from the substrate, we refer to this effect as bilayer blistering.</description><identifier>ISSN: 0006-3495</identifier><identifier>EISSN: 1542-0086</identifier><identifier>DOI: 10.1016/S0006-3495(99)77015-3</identifier><identifier>PMID: 10465778</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry ; Biochemistry ; Lipid Bilayers - chemistry ; Lipids ; Microscopy, Atomic Force - methods ; Models, Molecular ; Molecular Conformation ; Phosphatidylcholines - chemistry ; Phosphatidylethanolamines - chemistry ; Phosphatidylglycerols - chemistry ; Proteins ; Scientific imaging ; Structure-Activity Relationship</subject><ispartof>Biophysical journal, 1999-09, Vol.77 (3), p.1683-1693</ispartof><rights>1999 The Biophysical Society</rights><rights>Copyright Biophysical Society Sep 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-715cffa427b964a056ce023be5af09559ebd26ae55aff9ed246a01ec6c414e9b3</citedby><cites>FETCH-LOGICAL-c490t-715cffa427b964a056ce023be5af09559ebd26ae55aff9ed246a01ec6c414e9b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1300455/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0006-3495(99)77015-3$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,3537,27905,27906,45976,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10465778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rinia, Hilde A.</creatorcontrib><creatorcontrib>Demel, Rudy A.</creatorcontrib><creatorcontrib>van der Eerden, Jan P.J.M.</creatorcontrib><creatorcontrib>de Kruijff, Ben</creatorcontrib><title>Blistering of Langmuir-Blodgett Bilayers Containing Anionic Phospholipids as Observed by Atomic Force Microscopy</title><title>Biophysical journal</title><addtitle>Biophys J</addtitle><description>Asymmetric bilayers of different phospholipid compositions have been prepared by the Langmuir-Blodgett (L-B) method, and imaged by atomic force microscopy (AFM). Such bilayers can function as a model for biological membranes. The first leaflet consisted of zwitterionic phospholipids phosphatidylcholine (PC) or phosphatidylethanolamine (PE). The second leaflet consisted of the anionic phospholipid phosphatidylglycerol (PG), in either the condensed or liquid phase or, for comparison, of PC. Different bilayers showed different morphology. In all bilayers defects in the form of holes were present. In some bilayers with a first leaflet consisting of PC, polygonal line-shaped defects were observed, whereas when the first leaflet consisted of PE, mainly round defects were seen. Not only the shape, but also the amount of defects varied, depending on the condition and the composition of the second leaflet. In most of the PG-containing systems the defects were surrounded by elevations, which reversibly disappeared in the presence of divalent cations. This is the first time that such elevations have been observed on phospholipid bilayers. We propose that they are induced by phospholipid exchange between the two leaflets around the defects, leading to the presence of negatively charged phospholipids in the first leaflet. Because the substrate is also negatively charged, the bilayer around the edges is repelled and lifted up. Since it was found that the elevations are indeed detached from the substrate, we refer to this effect as bilayer blistering.</description><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry</subject><subject>Biochemistry</subject><subject>Lipid Bilayers - chemistry</subject><subject>Lipids</subject><subject>Microscopy, Atomic Force - methods</subject><subject>Models, Molecular</subject><subject>Molecular Conformation</subject><subject>Phosphatidylcholines - chemistry</subject><subject>Phosphatidylethanolamines - chemistry</subject><subject>Phosphatidylglycerols - chemistry</subject><subject>Proteins</subject><subject>Scientific imaging</subject><subject>Structure-Activity Relationship</subject><issn>0006-3495</issn><issn>1542-0086</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkUFv0zAUxy0EYt3gI4AsDggOgefEduoLqK0YIBUNCThbjvPSekrtzE4q9dvPXadpcMEXy_Lv_e33foS8YvCBAZMffwGALCquxDul3tc1MFFUT8iMCV4WAHP5lMwekDNyntI1ACsFsOfkjAGXoq7nMzIse5dGjM5vaOjo2vjNbnKxWPah3eA40qXrzQFjoqvgR-P8EVx4F7yz9Oc2pGEbeje4NlGT6FWTMO6xpc2BLsawy8xliBbpD2djSDYMhxfkWWf6hC_v9wvy5_LL79W3Yn319ftqsS4sVzAWNRO26wwv60ZJbkBIi1BWDQrTgRJCYdOW0qDI505hW3JpgKGVljOOqqkuyKdT7jA1O2wt-jGaXg_R7Uw86GCc_vvGu63ehL1mFQAXIge8vQ-I4WbCNOqdSxb73ngMU9JS5cX5PINv_gGvwxR9bk6XTNQlFyXLkDhBxzmkiN3DTxjoo1B9J1QfbWml9J1QXeW614_beFR1MpiBzycA8zD3DqNO1qG32LqIdtRtcP954hZGSLL1</recordid><startdate>19990901</startdate><enddate>19990901</enddate><creator>Rinia, Hilde A.</creator><creator>Demel, Rudy A.</creator><creator>van der Eerden, Jan P.J.M.</creator><creator>de Kruijff, Ben</creator><general>Elsevier Inc</general><general>Biophysical Society</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>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990901</creationdate><title>Blistering of Langmuir-Blodgett Bilayers Containing Anionic Phospholipids as Observed by Atomic Force Microscopy</title><author>Rinia, Hilde A. ; Demel, Rudy A. ; van der Eerden, Jan P.J.M. ; de Kruijff, Ben</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-715cffa427b964a056ce023be5af09559ebd26ae55aff9ed246a01ec6c414e9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>1,2-Dipalmitoylphosphatidylcholine - chemistry</topic><topic>Biochemistry</topic><topic>Lipid Bilayers - chemistry</topic><topic>Lipids</topic><topic>Microscopy, Atomic Force - methods</topic><topic>Models, Molecular</topic><topic>Molecular Conformation</topic><topic>Phosphatidylcholines - chemistry</topic><topic>Phosphatidylethanolamines - chemistry</topic><topic>Phosphatidylglycerols - chemistry</topic><topic>Proteins</topic><topic>Scientific imaging</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rinia, Hilde A.</creatorcontrib><creatorcontrib>Demel, Rudy A.</creatorcontrib><creatorcontrib>van der Eerden, Jan P.J.M.</creatorcontrib><creatorcontrib>de Kruijff, Ben</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>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biophysical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rinia, Hilde A.</au><au>Demel, Rudy A.</au><au>van der Eerden, Jan P.J.M.</au><au>de Kruijff, Ben</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blistering of Langmuir-Blodgett Bilayers Containing Anionic Phospholipids as Observed by Atomic Force Microscopy</atitle><jtitle>Biophysical journal</jtitle><addtitle>Biophys J</addtitle><date>1999-09-01</date><risdate>1999</risdate><volume>77</volume><issue>3</issue><spage>1683</spage><epage>1693</epage><pages>1683-1693</pages><issn>0006-3495</issn><eissn>1542-0086</eissn><abstract>Asymmetric bilayers of different phospholipid compositions have been prepared by the Langmuir-Blodgett (L-B) method, and imaged by atomic force microscopy (AFM). Such bilayers can function as a model for biological membranes. The first leaflet consisted of zwitterionic phospholipids phosphatidylcholine (PC) or phosphatidylethanolamine (PE). The second leaflet consisted of the anionic phospholipid phosphatidylglycerol (PG), in either the condensed or liquid phase or, for comparison, of PC. Different bilayers showed different morphology. In all bilayers defects in the form of holes were present. In some bilayers with a first leaflet consisting of PC, polygonal line-shaped defects were observed, whereas when the first leaflet consisted of PE, mainly round defects were seen. Not only the shape, but also the amount of defects varied, depending on the condition and the composition of the second leaflet. In most of the PG-containing systems the defects were surrounded by elevations, which reversibly disappeared in the presence of divalent cations. This is the first time that such elevations have been observed on phospholipid bilayers. We propose that they are induced by phospholipid exchange between the two leaflets around the defects, leading to the presence of negatively charged phospholipids in the first leaflet. Because the substrate is also negatively charged, the bilayer around the edges is repelled and lifted up. Since it was found that the elevations are indeed detached from the substrate, we refer to this effect as bilayer blistering.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10465778</pmid><doi>10.1016/S0006-3495(99)77015-3</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 1,2-Dipalmitoylphosphatidylcholine - chemistry Biochemistry Lipid Bilayers - chemistry Lipids Microscopy, Atomic Force - methods Models, Molecular Molecular Conformation Phosphatidylcholines - chemistry Phosphatidylethanolamines - chemistry Phosphatidylglycerols - chemistry Proteins Scientific imaging Structure-Activity Relationship |
title | Blistering of Langmuir-Blodgett Bilayers Containing Anionic Phospholipids as Observed by Atomic Force Microscopy |
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