Location and mobility of ubiquinones of different chain lengths in artificial membrane vesicles
Ubiquinone (UQn with n = 2, 3, or 10 isoprenoid groups) was incorporated into small, sonicated vesicles made of dipalmitoylphosphatidylcholine (DPPC) or dimyristoylphosphatidylcholine (DMPC). (1) The accessibility of oxidized UQ in DPPC or DMPC vesicles to the reductant sodium borohydride (NaBH4), m...
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Veröffentlicht in: | Biochemistry (Easton) 1985-05, Vol.24 (10), p.2501-2508 |
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creator | Ulrich, E. L Girvin, M. E Cramer, W. A Markley, J. L |
description | Ubiquinone (UQn with n = 2, 3, or 10 isoprenoid groups) was incorporated into small, sonicated vesicles made of dipalmitoylphosphatidylcholine (DPPC) or dimyristoylphosphatidylcholine (DMPC). (1) The accessibility of oxidized UQ in DPPC or DMPC vesicles to the reductant sodium borohydride (NaBH4), measured by UV spectroscopy, was UQ2 greater than UQ3 greater than UQ10 (DPPC) and UQ2 greater than UQ3 approximately UQ10 (DMPC). (2) Catalysis of the reduction of entrapped ferricyanide by exogenous NaBH4 was more effective with UQ2 than UQ10 but was slower with all quinones than reduction by added dithionite. (3) The methoxy protons of UQ2 and UQ3 in DPPC and DMPC vesicles exhibited a single NMR resonance centered at approximately 3.95 ppm, whereas the methoxy groups of UQ10 gave rise to two separate proton resonances, at 3.93 ppm and a more narrow resonance at 3.78 ppm. The UQ10 population characterized by the 3.78 ppm resonance was present at a higher concentration in DPPC than in DMPC vesicles and was relatively insensitive to reduction by NaBH4. (4) UQ10 perturbed the melting temperature (Tm) of DPPC vesicles to a smaller extent (delta Tm = -1 degrees C) than did UQ2 and UQ3 (delta Tm = -3 to -4 degrees C). The combined UV and NMR data imply the following: The UQ10 pool characterized by the 3.78 ppm peak corresponds to a more mobile UQ10 fraction that is not reduced by NaBH4 in 2-3 min and is thought to be localized close to the center of the DPPC bilayer since it has little effect on the DPPC Tm. |
doi_str_mv | 10.1021/bi00331a016 |
format | Article |
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L ; Girvin, M. E ; Cramer, W. A ; Markley, J. L</creator><creatorcontrib>Ulrich, E. L ; Girvin, M. E ; Cramer, W. A ; Markley, J. L</creatorcontrib><description>Ubiquinone (UQn with n = 2, 3, or 10 isoprenoid groups) was incorporated into small, sonicated vesicles made of dipalmitoylphosphatidylcholine (DPPC) or dimyristoylphosphatidylcholine (DMPC). (1) The accessibility of oxidized UQ in DPPC or DMPC vesicles to the reductant sodium borohydride (NaBH4), measured by UV spectroscopy, was UQ2 greater than UQ3 greater than UQ10 (DPPC) and UQ2 greater than UQ3 approximately UQ10 (DMPC). (2) Catalysis of the reduction of entrapped ferricyanide by exogenous NaBH4 was more effective with UQ2 than UQ10 but was slower with all quinones than reduction by added dithionite. (3) The methoxy protons of UQ2 and UQ3 in DPPC and DMPC vesicles exhibited a single NMR resonance centered at approximately 3.95 ppm, whereas the methoxy groups of UQ10 gave rise to two separate proton resonances, at 3.93 ppm and a more narrow resonance at 3.78 ppm. The UQ10 population characterized by the 3.78 ppm resonance was present at a higher concentration in DPPC than in DMPC vesicles and was relatively insensitive to reduction by NaBH4. (4) UQ10 perturbed the melting temperature (Tm) of DPPC vesicles to a smaller extent (delta Tm = -1 degrees C) than did UQ2 and UQ3 (delta Tm = -3 to -4 degrees C). The combined UV and NMR data imply the following: The UQ10 pool characterized by the 3.78 ppm peak corresponds to a more mobile UQ10 fraction that is not reduced by NaBH4 in 2-3 min and is thought to be localized close to the center of the DPPC bilayer since it has little effect on the DPPC Tm.</description><identifier>ISSN: 0006-2960</identifier><identifier>EISSN: 1520-4995</identifier><identifier>DOI: 10.1021/bi00331a016</identifier><identifier>PMID: 3839413</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Artificial membranes and reconstituted systems ; Biological and medical sciences ; Dimyristoylphosphatidylcholine ; Fundamental and applied biological sciences. Psychology ; Kinetics ; Liposomes ; Magnetic Resonance Spectroscopy ; Membrane physicochemistry ; Models, Biological ; Molecular biophysics ; Oxidation-Reduction ; Pulmonary Surfactants ; Structure-Activity Relationship ; Thermodynamics ; Ubiquinone ; ubiquinones</subject><ispartof>Biochemistry (Easton), 1985-05, Vol.24 (10), p.2501-2508</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a480t-c4f6a4159012e88399ad600f30988ce448029042767fa272c7e77d042a563a343</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/bi00331a016$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bi00331a016$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2764,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8475680$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3839413$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ulrich, E. L</creatorcontrib><creatorcontrib>Girvin, M. E</creatorcontrib><creatorcontrib>Cramer, W. A</creatorcontrib><creatorcontrib>Markley, J. L</creatorcontrib><title>Location and mobility of ubiquinones of different chain lengths in artificial membrane vesicles</title><title>Biochemistry (Easton)</title><addtitle>Biochemistry</addtitle><description>Ubiquinone (UQn with n = 2, 3, or 10 isoprenoid groups) was incorporated into small, sonicated vesicles made of dipalmitoylphosphatidylcholine (DPPC) or dimyristoylphosphatidylcholine (DMPC). (1) The accessibility of oxidized UQ in DPPC or DMPC vesicles to the reductant sodium borohydride (NaBH4), measured by UV spectroscopy, was UQ2 greater than UQ3 greater than UQ10 (DPPC) and UQ2 greater than UQ3 approximately UQ10 (DMPC). (2) Catalysis of the reduction of entrapped ferricyanide by exogenous NaBH4 was more effective with UQ2 than UQ10 but was slower with all quinones than reduction by added dithionite. (3) The methoxy protons of UQ2 and UQ3 in DPPC and DMPC vesicles exhibited a single NMR resonance centered at approximately 3.95 ppm, whereas the methoxy groups of UQ10 gave rise to two separate proton resonances, at 3.93 ppm and a more narrow resonance at 3.78 ppm. The UQ10 population characterized by the 3.78 ppm resonance was present at a higher concentration in DPPC than in DMPC vesicles and was relatively insensitive to reduction by NaBH4. (4) UQ10 perturbed the melting temperature (Tm) of DPPC vesicles to a smaller extent (delta Tm = -1 degrees C) than did UQ2 and UQ3 (delta Tm = -3 to -4 degrees C). The combined UV and NMR data imply the following: The UQ10 pool characterized by the 3.78 ppm peak corresponds to a more mobile UQ10 fraction that is not reduced by NaBH4 in 2-3 min and is thought to be localized close to the center of the DPPC bilayer since it has little effect on the DPPC Tm.</description><subject>Artificial membranes and reconstituted systems</subject><subject>Biological and medical sciences</subject><subject>Dimyristoylphosphatidylcholine</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kinetics</subject><subject>Liposomes</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Membrane physicochemistry</subject><subject>Models, Biological</subject><subject>Molecular biophysics</subject><subject>Oxidation-Reduction</subject><subject>Pulmonary Surfactants</subject><subject>Structure-Activity Relationship</subject><subject>Thermodynamics</subject><subject>Ubiquinone</subject><subject>ubiquinones</subject><issn>0006-2960</issn><issn>1520-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1rFTEUhoMo9VpduRZmIbqQ0ZOPSSbLWqwKFxR6BXfhTCaxqTNJm8yI_fem3MvFheAqOed9OLw8hDyn8JYCo--GAMA5RaDyAdnQjkErtO4ekg0AyJZpCY_Jk1Ku6yhAiRNywnuuBeUbYrbJ4hJSbDCOzZyGMIXlrkm-WYdwu4aYoiv34xi8d9nFpbFXGGIzufhjuSpN_WJegg824NTMbh4yRtf8ciXYyZWn5JHHqbhnh_eUfLv4sDv_1G6_fPx8frZtUfSwtFZ4iYJ2GihzfS2ncZQAnoPue-tEhZgGwZRUHpliVjmlxrrATnLkgp-SV_u7Nzndrq4sZg7FummqZdJajJIMNGf8vyAVvGO1QQXf7EGbUynZeXOTw4z5zlAw997NX94r_eJwdh1mNx7Zg-iavzzkWCxOvkqyoRyxXqhO9lCxdo-FsrjfxxjzTyMVV53Zfb008j3wy-5iZ75X_vWeR1vMdVpzrJL_WfAPW-CkXw</recordid><startdate>19850507</startdate><enddate>19850507</enddate><creator>Ulrich, E. L</creator><creator>Girvin, M. E</creator><creator>Cramer, W. A</creator><creator>Markley, J. L</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</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>19850507</creationdate><title>Location and mobility of ubiquinones of different chain lengths in artificial membrane vesicles</title><author>Ulrich, E. L ; Girvin, M. E ; Cramer, W. A ; Markley, J. L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a480t-c4f6a4159012e88399ad600f30988ce448029042767fa272c7e77d042a563a343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Artificial membranes and reconstituted systems</topic><topic>Biological and medical sciences</topic><topic>Dimyristoylphosphatidylcholine</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kinetics</topic><topic>Liposomes</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Membrane physicochemistry</topic><topic>Models, Biological</topic><topic>Molecular biophysics</topic><topic>Oxidation-Reduction</topic><topic>Pulmonary Surfactants</topic><topic>Structure-Activity Relationship</topic><topic>Thermodynamics</topic><topic>Ubiquinone</topic><topic>ubiquinones</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ulrich, E. L</creatorcontrib><creatorcontrib>Girvin, M. E</creatorcontrib><creatorcontrib>Cramer, W. A</creatorcontrib><creatorcontrib>Markley, J. L</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Ulrich, E. L</au><au>Girvin, M. E</au><au>Cramer, W. A</au><au>Markley, J. L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Location and mobility of ubiquinones of different chain lengths in artificial membrane vesicles</atitle><jtitle>Biochemistry (Easton)</jtitle><addtitle>Biochemistry</addtitle><date>1985-05-07</date><risdate>1985</risdate><volume>24</volume><issue>10</issue><spage>2501</spage><epage>2508</epage><pages>2501-2508</pages><issn>0006-2960</issn><eissn>1520-4995</eissn><abstract>Ubiquinone (UQn with n = 2, 3, or 10 isoprenoid groups) was incorporated into small, sonicated vesicles made of dipalmitoylphosphatidylcholine (DPPC) or dimyristoylphosphatidylcholine (DMPC). (1) The accessibility of oxidized UQ in DPPC or DMPC vesicles to the reductant sodium borohydride (NaBH4), measured by UV spectroscopy, was UQ2 greater than UQ3 greater than UQ10 (DPPC) and UQ2 greater than UQ3 approximately UQ10 (DMPC). (2) Catalysis of the reduction of entrapped ferricyanide by exogenous NaBH4 was more effective with UQ2 than UQ10 but was slower with all quinones than reduction by added dithionite. (3) The methoxy protons of UQ2 and UQ3 in DPPC and DMPC vesicles exhibited a single NMR resonance centered at approximately 3.95 ppm, whereas the methoxy groups of UQ10 gave rise to two separate proton resonances, at 3.93 ppm and a more narrow resonance at 3.78 ppm. The UQ10 population characterized by the 3.78 ppm resonance was present at a higher concentration in DPPC than in DMPC vesicles and was relatively insensitive to reduction by NaBH4. (4) UQ10 perturbed the melting temperature (Tm) of DPPC vesicles to a smaller extent (delta Tm = -1 degrees C) than did UQ2 and UQ3 (delta Tm = -3 to -4 degrees C). The combined UV and NMR data imply the following: The UQ10 pool characterized by the 3.78 ppm peak corresponds to a more mobile UQ10 fraction that is not reduced by NaBH4 in 2-3 min and is thought to be localized close to the center of the DPPC bilayer since it has little effect on the DPPC Tm.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>3839413</pmid><doi>10.1021/bi00331a016</doi><tpages>8</tpages></addata></record> |
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subjects | Artificial membranes and reconstituted systems Biological and medical sciences Dimyristoylphosphatidylcholine Fundamental and applied biological sciences. Psychology Kinetics Liposomes Magnetic Resonance Spectroscopy Membrane physicochemistry Models, Biological Molecular biophysics Oxidation-Reduction Pulmonary Surfactants Structure-Activity Relationship Thermodynamics Ubiquinone ubiquinones |
title | Location and mobility of ubiquinones of different chain lengths in artificial membrane vesicles |
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