Abolition of the thermotropic transition of charged phospholipids induced by a cardiotoxin from Naja mossambica mossambica as detected by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy

The effects of a Naja mossambica mossambica cardiotoxin on the thermotropic properties of charged phospholipids have been studied by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy. The binding of the toxin is only governed by the net charge at the interface and...

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Veröffentlicht in:Biochemistry (Easton) 1983-04, Vol.22 (9), p.2179-2185
Hauptverfasser: Faucon, Jean Francois, Dufourcq, Jean, Bernard, Evelyne, Duchesneau, Luc, Pezolet, Michel
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container_issue 9
container_start_page 2179
container_title Biochemistry (Easton)
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creator Faucon, Jean Francois
Dufourcq, Jean
Bernard, Evelyne
Duchesneau, Luc
Pezolet, Michel
description The effects of a Naja mossambica mossambica cardiotoxin on the thermotropic properties of charged phospholipids have been studied by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy. The binding of the toxin is only governed by the net charge at the interface and is not affected by the polar head group structure of the phospholipids or by the acyl chains physical state, degree of insaturation, or length. The effect of the toxin on the phospholipid structure is drastic. In all cases, the gel to liquid-crystalline phase transition monitored by fluorescence and Raman spectroscopies is progressively abolished without notable shift in temperature as the proportion of toxin is increased. The endothermic peaks detected by differential scanning calorimetry decrease in intensity as the toxin content is increased but always remain sharp. All the techniques used give complementary results, and none of them reveals the presence of secondary transitions at higher or lower temperatures. We thus believe that the lipid molecules that are perturbed by the toxin, approximately 10 +/- 2 molecules, do not undergo a phase transition. Raman results demonstrate that these "boundary" lipids display a population of gauche rotamers that is as high as the one found in the liquid-crystalline phase of the pure phospholipid and this even well below the phase transition temperature. On the other hand, fluorescence results are interpreted as due to a partial immobilization of the lipids in contact with the toxin above the transition temperature. Thus, even though the interaction is governed by electrostatic forces, the toxin penetrates at least partially into the bilayers, inducing a disorganization of the aliphatic chains and changes in their mobility; this could explain their lytic activity.
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The binding of the toxin is only governed by the net charge at the interface and is not affected by the polar head group structure of the phospholipids or by the acyl chains physical state, degree of insaturation, or length. The effect of the toxin on the phospholipid structure is drastic. In all cases, the gel to liquid-crystalline phase transition monitored by fluorescence and Raman spectroscopies is progressively abolished without notable shift in temperature as the proportion of toxin is increased. The endothermic peaks detected by differential scanning calorimetry decrease in intensity as the toxin content is increased but always remain sharp. All the techniques used give complementary results, and none of them reveals the presence of secondary transitions at higher or lower temperatures. We thus believe that the lipid molecules that are perturbed by the toxin, approximately 10 +/- 2 molecules, do not undergo a phase transition. Raman results demonstrate that these "boundary" lipids display a population of gauche rotamers that is as high as the one found in the liquid-crystalline phase of the pure phospholipid and this even well below the phase transition temperature. On the other hand, fluorescence results are interpreted as due to a partial immobilization of the lipids in contact with the toxin above the transition temperature. Thus, even though the interaction is governed by electrostatic forces, the toxin penetrates at least partially into the bilayers, inducing a disorganization of the aliphatic chains and changes in their mobility; this could explain their lytic activity.</description><identifier>ISSN: 0006-2960</identifier><identifier>EISSN: 1520-4995</identifier><identifier>DOI: 10.1021/bi00278a019</identifier><identifier>PMID: 6860658</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Calorimetry, Differential Scanning ; cardiotoxins ; Cobra Cardiotoxin Proteins ; differential scanning calorimetry ; Elapid Venoms ; fluorescence ; Kinetics ; Liposomes ; Molecular Conformation ; Naja mossambica mossambica ; phase transition ; Phospholipids ; Raman spectroscopy ; Spectrometry, Fluorescence ; Spectrum Analysis, Raman ; Structure-Activity Relationship ; Temperature</subject><ispartof>Biochemistry (Easton), 1983-04, Vol.22 (9), p.2179-2185</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a385t-31ac1e07f2e556ca364a6fb56022103499d1bdb3f16e2b6c6b2b31959189ccc33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bi00278a019$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bi00278a019$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6860658$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Faucon, Jean Francois</creatorcontrib><creatorcontrib>Dufourcq, Jean</creatorcontrib><creatorcontrib>Bernard, Evelyne</creatorcontrib><creatorcontrib>Duchesneau, Luc</creatorcontrib><creatorcontrib>Pezolet, Michel</creatorcontrib><title>Abolition of the thermotropic transition of charged phospholipids induced by a cardiotoxin from Naja mossambica mossambica as detected by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy</title><title>Biochemistry (Easton)</title><addtitle>Biochemistry</addtitle><description>The effects of a Naja mossambica mossambica cardiotoxin on the thermotropic properties of charged phospholipids have been studied by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy. The binding of the toxin is only governed by the net charge at the interface and is not affected by the polar head group structure of the phospholipids or by the acyl chains physical state, degree of insaturation, or length. The effect of the toxin on the phospholipid structure is drastic. In all cases, the gel to liquid-crystalline phase transition monitored by fluorescence and Raman spectroscopies is progressively abolished without notable shift in temperature as the proportion of toxin is increased. The endothermic peaks detected by differential scanning calorimetry decrease in intensity as the toxin content is increased but always remain sharp. All the techniques used give complementary results, and none of them reveals the presence of secondary transitions at higher or lower temperatures. We thus believe that the lipid molecules that are perturbed by the toxin, approximately 10 +/- 2 molecules, do not undergo a phase transition. Raman results demonstrate that these "boundary" lipids display a population of gauche rotamers that is as high as the one found in the liquid-crystalline phase of the pure phospholipid and this even well below the phase transition temperature. On the other hand, fluorescence results are interpreted as due to a partial immobilization of the lipids in contact with the toxin above the transition temperature. Thus, even though the interaction is governed by electrostatic forces, the toxin penetrates at least partially into the bilayers, inducing a disorganization of the aliphatic chains and changes in their mobility; this could explain their lytic activity.</description><subject>Animals</subject><subject>Calorimetry, Differential Scanning</subject><subject>cardiotoxins</subject><subject>Cobra Cardiotoxin Proteins</subject><subject>differential scanning calorimetry</subject><subject>Elapid Venoms</subject><subject>fluorescence</subject><subject>Kinetics</subject><subject>Liposomes</subject><subject>Molecular Conformation</subject><subject>Naja mossambica mossambica</subject><subject>phase transition</subject><subject>Phospholipids</subject><subject>Raman spectroscopy</subject><subject>Spectrometry, Fluorescence</subject><subject>Spectrum Analysis, Raman</subject><subject>Structure-Activity Relationship</subject><subject>Temperature</subject><issn>0006-2960</issn><issn>1520-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU2LFDEUDKKs4-rJs5CTHtzWfEzS3cdlcVUcV9EVj-Elnd7J2J30JmnY8cf6W8www6AgeHjko-pV8V4h9JSSV5Qw-lo7QljdAKHtPbSggpFq2bbiPloQQmTFWkkeokcpbcpzSerlCTqRjSRSNAv061yHwWUXPA49zmu7qziGHMPkDM4RfDrCZg3xxnZ4WodUanCT6xJ2vptN-dVbDNhA7FzI4c553Mcw4ivYAB5DSjBqZ_66QsKdzdbkfXM_zCHaZKw3Fk9hgOh-ws76DHeu7220PjsYcDLgvfM3xWsI0Y02x-0ZBt_hLzCCx2kqkjEkE6btY_SghyHZJ4fzFH27fHN98a5afXr7_uJ8VQFvRK44BUMtqXtmhZAGuFyC7LWQhDFKeNlmR3WneU-lZVoaqZnmtBUtbVpjDOen6Pled4rhdrYpq9GVSYYBvA1zUg0RjJXV_5dIuWhawXeKL_dEU0ZJ0fZqKrNC3CpK1C529Ufshf3sIDvr0XZH7iHngld73KVs744wxB9K1rwW6vrzV7X6eHn14XvNFCv8F3s-mKQ2YY6-bO-fzr8BwZPKLg</recordid><startdate>19830426</startdate><enddate>19830426</enddate><creator>Faucon, Jean Francois</creator><creator>Dufourcq, Jean</creator><creator>Bernard, Evelyne</creator><creator>Duchesneau, Luc</creator><creator>Pezolet, Michel</creator><general>American Chemical Society</general><scope>BSCLL</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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19830426</creationdate><title>Abolition of the thermotropic transition of charged phospholipids induced by a cardiotoxin from Naja mossambica mossambica as detected by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy</title><author>Faucon, Jean Francois ; Dufourcq, Jean ; Bernard, Evelyne ; Duchesneau, Luc ; Pezolet, Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a385t-31ac1e07f2e556ca364a6fb56022103499d1bdb3f16e2b6c6b2b31959189ccc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Animals</topic><topic>Calorimetry, Differential Scanning</topic><topic>cardiotoxins</topic><topic>Cobra Cardiotoxin Proteins</topic><topic>differential scanning calorimetry</topic><topic>Elapid Venoms</topic><topic>fluorescence</topic><topic>Kinetics</topic><topic>Liposomes</topic><topic>Molecular Conformation</topic><topic>Naja mossambica mossambica</topic><topic>phase transition</topic><topic>Phospholipids</topic><topic>Raman spectroscopy</topic><topic>Spectrometry, Fluorescence</topic><topic>Spectrum Analysis, Raman</topic><topic>Structure-Activity Relationship</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Faucon, Jean Francois</creatorcontrib><creatorcontrib>Dufourcq, Jean</creatorcontrib><creatorcontrib>Bernard, Evelyne</creatorcontrib><creatorcontrib>Duchesneau, Luc</creatorcontrib><creatorcontrib>Pezolet, Michel</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemistry (Easton)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Faucon, Jean Francois</au><au>Dufourcq, Jean</au><au>Bernard, Evelyne</au><au>Duchesneau, Luc</au><au>Pezolet, Michel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abolition of the thermotropic transition of charged phospholipids induced by a cardiotoxin from Naja mossambica mossambica as detected by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy</atitle><jtitle>Biochemistry (Easton)</jtitle><addtitle>Biochemistry</addtitle><date>1983-04-26</date><risdate>1983</risdate><volume>22</volume><issue>9</issue><spage>2179</spage><epage>2185</epage><pages>2179-2185</pages><issn>0006-2960</issn><eissn>1520-4995</eissn><abstract>The effects of a Naja mossambica mossambica cardiotoxin on the thermotropic properties of charged phospholipids have been studied by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy. The binding of the toxin is only governed by the net charge at the interface and is not affected by the polar head group structure of the phospholipids or by the acyl chains physical state, degree of insaturation, or length. The effect of the toxin on the phospholipid structure is drastic. In all cases, the gel to liquid-crystalline phase transition monitored by fluorescence and Raman spectroscopies is progressively abolished without notable shift in temperature as the proportion of toxin is increased. The endothermic peaks detected by differential scanning calorimetry decrease in intensity as the toxin content is increased but always remain sharp. All the techniques used give complementary results, and none of them reveals the presence of secondary transitions at higher or lower temperatures. We thus believe that the lipid molecules that are perturbed by the toxin, approximately 10 +/- 2 molecules, do not undergo a phase transition. Raman results demonstrate that these "boundary" lipids display a population of gauche rotamers that is as high as the one found in the liquid-crystalline phase of the pure phospholipid and this even well below the phase transition temperature. On the other hand, fluorescence results are interpreted as due to a partial immobilization of the lipids in contact with the toxin above the transition temperature. Thus, even though the interaction is governed by electrostatic forces, the toxin penetrates at least partially into the bilayers, inducing a disorganization of the aliphatic chains and changes in their mobility; this could explain their lytic activity.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>6860658</pmid><doi>10.1021/bi00278a019</doi><tpages>7</tpages></addata></record>
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source MEDLINE; American Chemical Society Journals
subjects Animals
Calorimetry, Differential Scanning
cardiotoxins
Cobra Cardiotoxin Proteins
differential scanning calorimetry
Elapid Venoms
fluorescence
Kinetics
Liposomes
Molecular Conformation
Naja mossambica mossambica
phase transition
Phospholipids
Raman spectroscopy
Spectrometry, Fluorescence
Spectrum Analysis, Raman
Structure-Activity Relationship
Temperature
title Abolition of the thermotropic transition of charged phospholipids induced by a cardiotoxin from Naja mossambica mossambica as detected by fluorescence polarization, differential scanning calorimetry, and Raman spectroscopy
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