Quantitative Determination of Luminal and Abluminal Membrane Distributions of Transporters in Porcine Brain Capillaries by Plasma Membrane Fractionation and Quantitative Targeted Proteomics
Abluminal or luminal localization of transporter in plasma membranes at the blood–brain barrier (BBB) is critical for their physiological and pharmacological roles. Therefore, the purpose of this study was to develop a new method to investigate membrane localization of transporters, through quantita...
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Veröffentlicht in: | Journal of pharmaceutical sciences 2015-09, Vol.104 (9), p.3060-3068 |
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description | Abluminal or luminal localization of transporter in plasma membranes at the blood–brain barrier (BBB) is critical for their physiological and pharmacological roles. Therefore, the purpose of this study was to develop a new method to investigate membrane localization of transporters, through quantitative measurement of protein expression levels in fractionated plasma membrane prepared from porcine brain capillaries. Luminal–abluminal distribution ratios were calculated from the results of quantitative targeted absolute proteomics of fractionated membranes, after correction for cross-contamination based on measurements of luminal and abluminal membrane markers. BCRP expression was greater at the luminal membrane than at the abluminal membrane, supporting the usefulness of the distribution ratio as a quantitative indicator of localization. The distribution ratios suggested luminal-dominant localizations of GLUT1 and OATP3A1, and abluminal-dominant localizations of ABCA1 and FATP1. For OATP3A1, ABCA1 and FATP1, these results require reconsideration of their functions at the BBB. Species differences were examined using expression levels normalized to Na+/K+–ATPase. BCRP expression is dominant over multidrug resistance 1 expression in porcine BBB, as in other primates including humans. This methodology for quantitative measurement of protein localization is expected to improve our understanding of the roles of transporters at the BBB, and should be applicable to other polarized cells. |
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Therefore, the purpose of this study was to develop a new method to investigate membrane localization of transporters, through quantitative measurement of protein expression levels in fractionated plasma membrane prepared from porcine brain capillaries. Luminal–abluminal distribution ratios were calculated from the results of quantitative targeted absolute proteomics of fractionated membranes, after correction for cross-contamination based on measurements of luminal and abluminal membrane markers. BCRP expression was greater at the luminal membrane than at the abluminal membrane, supporting the usefulness of the distribution ratio as a quantitative indicator of localization. The distribution ratios suggested luminal-dominant localizations of GLUT1 and OATP3A1, and abluminal-dominant localizations of ABCA1 and FATP1. For OATP3A1, ABCA1 and FATP1, these results require reconsideration of their functions at the BBB. Species differences were examined using expression levels normalized to Na+/K+–ATPase. BCRP expression is dominant over multidrug resistance 1 expression in porcine BBB, as in other primates including humans. This methodology for quantitative measurement of protein localization is expected to improve our understanding of the roles of transporters at the BBB, and should be applicable to other polarized cells.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.24398</identifier><identifier>PMID: 25703048</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; ATP Binding Cassette Transporter 1 - metabolism ; ATP-Binding Cassette Transporters - metabolism ; Biological Transport - physiology ; Blood-Brain Barrier - metabolism ; blood–brain barrier ; Brain - metabolism ; Capillaries - metabolism ; Cell Membrane - metabolism ; Fatty Acid Transport Proteins - metabolism ; Glucose Transporter Type 1 - metabolism ; localization ; mass spectrometry ; membrane transport ; Membrane Transport Proteins - metabolism ; Organic Anion Transporters - metabolism ; pharmacoproteomics (PPx) ; polarity ; Proteomics - methods ; quantitative targeted absolute proteomics (QTAP) ; Sodium-Potassium-Exchanging ATPase - metabolism ; species differences ; Swine ; transporter</subject><ispartof>Journal of pharmaceutical sciences, 2015-09, Vol.104 (9), p.3060-3068</ispartof><rights>2015 Wiley Periodicals, Inc. and the American Pharmacists Association</rights><rights>2015 Wiley Periodicals, Inc. and the American Pharmacists Association.</rights><rights>Copyright © 2015 Wiley Periodicals, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6018-1f9e0fa677839c9aa3ed3f932533627d5721aa4cf251c57c31d5cb14e47195b73</citedby><cites>FETCH-LOGICAL-c6018-1f9e0fa677839c9aa3ed3f932533627d5721aa4cf251c57c31d5cb14e47195b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.24398$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.24398$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25703048$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kubo, Yoshiyuki</creatorcontrib><creatorcontrib>Ohtsuki, Sumio</creatorcontrib><creatorcontrib>Uchida, Yasuo</creatorcontrib><creatorcontrib>Terasaki, Tetsuya</creatorcontrib><title>Quantitative Determination of Luminal and Abluminal Membrane Distributions of Transporters in Porcine Brain Capillaries by Plasma Membrane Fractionation and Quantitative Targeted Proteomics</title><title>Journal of pharmaceutical sciences</title><addtitle>J Pharm Sci</addtitle><description>Abluminal or luminal localization of transporter in plasma membranes at the blood–brain barrier (BBB) is critical for their physiological and pharmacological roles. Therefore, the purpose of this study was to develop a new method to investigate membrane localization of transporters, through quantitative measurement of protein expression levels in fractionated plasma membrane prepared from porcine brain capillaries. Luminal–abluminal distribution ratios were calculated from the results of quantitative targeted absolute proteomics of fractionated membranes, after correction for cross-contamination based on measurements of luminal and abluminal membrane markers. BCRP expression was greater at the luminal membrane than at the abluminal membrane, supporting the usefulness of the distribution ratio as a quantitative indicator of localization. The distribution ratios suggested luminal-dominant localizations of GLUT1 and OATP3A1, and abluminal-dominant localizations of ABCA1 and FATP1. For OATP3A1, ABCA1 and FATP1, these results require reconsideration of their functions at the BBB. Species differences were examined using expression levels normalized to Na+/K+–ATPase. BCRP expression is dominant over multidrug resistance 1 expression in porcine BBB, as in other primates including humans. This methodology for quantitative measurement of protein localization is expected to improve our understanding of the roles of transporters at the BBB, and should be applicable to other polarized cells.</description><subject>Animals</subject><subject>ATP Binding Cassette Transporter 1 - metabolism</subject><subject>ATP-Binding Cassette Transporters - metabolism</subject><subject>Biological Transport - physiology</subject><subject>Blood-Brain Barrier - metabolism</subject><subject>blood–brain barrier</subject><subject>Brain - metabolism</subject><subject>Capillaries - metabolism</subject><subject>Cell Membrane - metabolism</subject><subject>Fatty Acid Transport Proteins - metabolism</subject><subject>Glucose Transporter Type 1 - metabolism</subject><subject>localization</subject><subject>mass spectrometry</subject><subject>membrane transport</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Organic Anion Transporters - metabolism</subject><subject>pharmacoproteomics (PPx)</subject><subject>polarity</subject><subject>Proteomics - methods</subject><subject>quantitative targeted absolute proteomics (QTAP)</subject><subject>Sodium-Potassium-Exchanging ATPase - metabolism</subject><subject>species differences</subject><subject>Swine</subject><subject>transporter</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS0EotPCghdAkdjQRVr_xvGyDJQfDWIQw9pynBvkURIHOymah-PdcJopCAQSK-v4fj73-h6EnhB8QTCml_shXlDOVHkPrYigOC8wkffRKtVozgRXJ-g0xj3GuMBCPEQnVEjMMC9X6PvHyfSjG83obiB7CSOEzvVJ-T7zTbaZZtVmpq-zq6o9qvfQVcH0iXdxDK6aZjzO_C5dx8GHZBMz12dbH6xL4ItgklqbwbWtCQ5iVh2ybWtiZ365XQdjZ6el-9zyt-F2JnxJ89XZNvgRfOdsfIQeNKaN8Ph4nqHP16926zf55sPrt-urTW7TJsqcNApwYwopS6asMoZBzRrFqGCsoLIWkhJjuG2oIFZIy0gtbEU4cEmUqCQ7Q88X3yH4rxPEUXcuWkh_6cFPUROJFSmVKMn_oJzxkiie0Gd_oHs_hbTgW4rxQlDGEnW-UDb4GAM0egiuM-GgCdZz_DrFr2_jT-zTo-NUdVD_JO_yTsDlAnxzLRz-7aTfbT_dWbLlBaT93jgIOloHvYXaBbCjrr37yyA_AN9bzlw</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Kubo, Yoshiyuki</creator><creator>Ohtsuki, Sumio</creator><creator>Uchida, Yasuo</creator><creator>Terasaki, Tetsuya</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201509</creationdate><title>Quantitative Determination of Luminal and Abluminal Membrane Distributions of Transporters in Porcine Brain Capillaries by Plasma Membrane Fractionation and Quantitative Targeted Proteomics</title><author>Kubo, Yoshiyuki ; Ohtsuki, Sumio ; Uchida, Yasuo ; Terasaki, Tetsuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6018-1f9e0fa677839c9aa3ed3f932533627d5721aa4cf251c57c31d5cb14e47195b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>ATP Binding Cassette Transporter 1 - metabolism</topic><topic>ATP-Binding Cassette Transporters - metabolism</topic><topic>Biological Transport - physiology</topic><topic>Blood-Brain Barrier - metabolism</topic><topic>blood–brain barrier</topic><topic>Brain - metabolism</topic><topic>Capillaries - metabolism</topic><topic>Cell Membrane - metabolism</topic><topic>Fatty Acid Transport Proteins - metabolism</topic><topic>Glucose Transporter Type 1 - metabolism</topic><topic>localization</topic><topic>mass spectrometry</topic><topic>membrane transport</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Organic Anion Transporters - metabolism</topic><topic>pharmacoproteomics (PPx)</topic><topic>polarity</topic><topic>Proteomics - methods</topic><topic>quantitative targeted absolute proteomics (QTAP)</topic><topic>Sodium-Potassium-Exchanging ATPase - metabolism</topic><topic>species differences</topic><topic>Swine</topic><topic>transporter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kubo, Yoshiyuki</creatorcontrib><creatorcontrib>Ohtsuki, Sumio</creatorcontrib><creatorcontrib>Uchida, Yasuo</creatorcontrib><creatorcontrib>Terasaki, Tetsuya</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kubo, Yoshiyuki</au><au>Ohtsuki, Sumio</au><au>Uchida, Yasuo</au><au>Terasaki, Tetsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative Determination of Luminal and Abluminal Membrane Distributions of Transporters in Porcine Brain Capillaries by Plasma Membrane Fractionation and Quantitative Targeted Proteomics</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J Pharm Sci</addtitle><date>2015-09</date><risdate>2015</risdate><volume>104</volume><issue>9</issue><spage>3060</spage><epage>3068</epage><pages>3060-3068</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>Abluminal or luminal localization of transporter in plasma membranes at the blood–brain barrier (BBB) is critical for their physiological and pharmacological roles. Therefore, the purpose of this study was to develop a new method to investigate membrane localization of transporters, through quantitative measurement of protein expression levels in fractionated plasma membrane prepared from porcine brain capillaries. Luminal–abluminal distribution ratios were calculated from the results of quantitative targeted absolute proteomics of fractionated membranes, after correction for cross-contamination based on measurements of luminal and abluminal membrane markers. BCRP expression was greater at the luminal membrane than at the abluminal membrane, supporting the usefulness of the distribution ratio as a quantitative indicator of localization. The distribution ratios suggested luminal-dominant localizations of GLUT1 and OATP3A1, and abluminal-dominant localizations of ABCA1 and FATP1. For OATP3A1, ABCA1 and FATP1, these results require reconsideration of their functions at the BBB. Species differences were examined using expression levels normalized to Na+/K+–ATPase. BCRP expression is dominant over multidrug resistance 1 expression in porcine BBB, as in other primates including humans. This methodology for quantitative measurement of protein localization is expected to improve our understanding of the roles of transporters at the BBB, and should be applicable to other polarized cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25703048</pmid><doi>10.1002/jps.24398</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals ATP Binding Cassette Transporter 1 - metabolism ATP-Binding Cassette Transporters - metabolism Biological Transport - physiology Blood-Brain Barrier - metabolism blood–brain barrier Brain - metabolism Capillaries - metabolism Cell Membrane - metabolism Fatty Acid Transport Proteins - metabolism Glucose Transporter Type 1 - metabolism localization mass spectrometry membrane transport Membrane Transport Proteins - metabolism Organic Anion Transporters - metabolism pharmacoproteomics (PPx) polarity Proteomics - methods quantitative targeted absolute proteomics (QTAP) Sodium-Potassium-Exchanging ATPase - metabolism species differences Swine transporter |
title | Quantitative Determination of Luminal and Abluminal Membrane Distributions of Transporters in Porcine Brain Capillaries by Plasma Membrane Fractionation and Quantitative Targeted Proteomics |
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