A micropreparation of mitochondria from cells using magnetic beads with immunoaffinity
Mitochondrial preparation is a key technique in the study of mitochondria. Growing evidence has demonstrated that mitochondrial proteins are tissue or cell type dependent. Locating the proteins in the global presence of mitochondrial membranes is a primary consideration in adopting antibodies for af...
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description | Mitochondrial preparation is a key technique in the study of mitochondria. Growing evidence has demonstrated that mitochondrial proteins are tissue or cell type dependent. Locating the proteins in the global presence of mitochondrial membranes is a primary consideration in adopting antibodies for affinity enrichment of mitochondria on a micro scale. Two proteins located on the outer membrane of mitochondria, cytochrome b5 type B (CYB5B) and synaptojanin-2-binding protein (SYNJ2BP), were selected as candidates based on a survey of databases and the literature. The polyclonal antibodies against the truncated CYB5B and SYNJ2BP exhibited specific recognition to mitochondria and wider sensitivity to several tested mouse tissues and cell lines, whereas the antibody 22-kDa translocase of the outer mitochondrial membrane (TOM22) nearly missed detection of mitochondria in the liver and responded minimally to mitochondria from H9C2 and L-02 cells. Through the affinity enrichment for cellular mitochondria using magnetic beads coated with anti-CYB5B or anti-SYNJ2BP, we found that the anti-CYB5B beads could enrich mitochondria more efficiently even on a scale of 10,000 cultured cells. For the integrity and protein components, the enriched mitochondria on anti-CYB5B were carefully examined and were accepted in further functional study. We propose that an anti-CYB5B immunomagnetic approach is feasible in the micropreparation of mitochondria from cultured cells. |
doi_str_mv | 10.1016/j.ab.2011.11.015 |
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Growing evidence has demonstrated that mitochondrial proteins are tissue or cell type dependent. Locating the proteins in the global presence of mitochondrial membranes is a primary consideration in adopting antibodies for affinity enrichment of mitochondria on a micro scale. Two proteins located on the outer membrane of mitochondria, cytochrome b5 type B (CYB5B) and synaptojanin-2-binding protein (SYNJ2BP), were selected as candidates based on a survey of databases and the literature. The polyclonal antibodies against the truncated CYB5B and SYNJ2BP exhibited specific recognition to mitochondria and wider sensitivity to several tested mouse tissues and cell lines, whereas the antibody 22-kDa translocase of the outer mitochondrial membrane (TOM22) nearly missed detection of mitochondria in the liver and responded minimally to mitochondria from H9C2 and L-02 cells. Through the affinity enrichment for cellular mitochondria using magnetic beads coated with anti-CYB5B or anti-SYNJ2BP, we found that the anti-CYB5B beads could enrich mitochondria more efficiently even on a scale of 10,000 cultured cells. For the integrity and protein components, the enriched mitochondria on anti-CYB5B were carefully examined and were accepted in further functional study. We propose that an anti-CYB5B immunomagnetic approach is feasible in the micropreparation of mitochondria from cultured cells.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2011.11.015</identifier><identifier>PMID: 22178913</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adaptor Proteins, Signal Transducing - genetics ; Adaptor Proteins, Signal Transducing - immunology ; Animals ; Antibody Affinity ; Base Sequence ; Cell Fractionation - methods ; Cell Fractionation - standards ; Cell Line ; cultured cells ; Cytochrome b5 type B (CYB5B) ; Cytochromes b5 - genetics ; Cytochromes b5 - immunology ; DNA Primers - genetics ; Immunomagnetic beads ; Immunomagnetic Separation - methods ; Immunomagnetic Separation - standards ; liver ; Membrane Proteins - genetics ; Membrane Proteins - immunology ; Mice ; mitochondria ; Mitochondria - chemistry ; Mitochondria - immunology ; Mitochondria isolation ; mitochondrial membrane ; Peptide Fragments - genetics ; Peptide Fragments - immunology ; polyclonal antibodies ; proteins ; Proteomics - methods ; Quality Control ; Recombinant Proteins - genetics ; Recombinant Proteins - immunology ; surveys ; Tissue-independent mitochondrial protein ; tissues</subject><ispartof>Analytical biochemistry, 2012-02, Vol.421 (1), p.219-226</ispartof><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-d039c526c2a20e473db73e285df3326c0026809109e15f73872326b12cdaea893</citedby><cites>FETCH-LOGICAL-c373t-d039c526c2a20e473db73e285df3326c0026809109e15f73872326b12cdaea893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ab.2011.11.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22178913$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ru, Yawei</creatorcontrib><creatorcontrib>Yin, Liang</creatorcontrib><creatorcontrib>Sun, Haidan</creatorcontrib><creatorcontrib>Yin, Songyue</creatorcontrib><creatorcontrib>Pan, Qin</creatorcontrib><creatorcontrib>Wei, Hanfu</creatorcontrib><creatorcontrib>Wu, Lin</creatorcontrib><creatorcontrib>Liu, Siqi</creatorcontrib><title>A micropreparation of mitochondria from cells using magnetic beads with immunoaffinity</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>Mitochondrial preparation is a key technique in the study of mitochondria. Growing evidence has demonstrated that mitochondrial proteins are tissue or cell type dependent. Locating the proteins in the global presence of mitochondrial membranes is a primary consideration in adopting antibodies for affinity enrichment of mitochondria on a micro scale. Two proteins located on the outer membrane of mitochondria, cytochrome b5 type B (CYB5B) and synaptojanin-2-binding protein (SYNJ2BP), were selected as candidates based on a survey of databases and the literature. The polyclonal antibodies against the truncated CYB5B and SYNJ2BP exhibited specific recognition to mitochondria and wider sensitivity to several tested mouse tissues and cell lines, whereas the antibody 22-kDa translocase of the outer mitochondrial membrane (TOM22) nearly missed detection of mitochondria in the liver and responded minimally to mitochondria from H9C2 and L-02 cells. Through the affinity enrichment for cellular mitochondria using magnetic beads coated with anti-CYB5B or anti-SYNJ2BP, we found that the anti-CYB5B beads could enrich mitochondria more efficiently even on a scale of 10,000 cultured cells. For the integrity and protein components, the enriched mitochondria on anti-CYB5B were carefully examined and were accepted in further functional study. We propose that an anti-CYB5B immunomagnetic approach is feasible in the micropreparation of mitochondria from cultured cells.</description><subject>Adaptor Proteins, Signal Transducing - genetics</subject><subject>Adaptor Proteins, Signal Transducing - immunology</subject><subject>Animals</subject><subject>Antibody Affinity</subject><subject>Base Sequence</subject><subject>Cell Fractionation - methods</subject><subject>Cell Fractionation - standards</subject><subject>Cell Line</subject><subject>cultured cells</subject><subject>Cytochrome b5 type B (CYB5B)</subject><subject>Cytochromes b5 - genetics</subject><subject>Cytochromes b5 - immunology</subject><subject>DNA Primers - genetics</subject><subject>Immunomagnetic beads</subject><subject>Immunomagnetic Separation - methods</subject><subject>Immunomagnetic Separation - standards</subject><subject>liver</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - immunology</subject><subject>Mice</subject><subject>mitochondria</subject><subject>Mitochondria - chemistry</subject><subject>Mitochondria - immunology</subject><subject>Mitochondria isolation</subject><subject>mitochondrial membrane</subject><subject>Peptide Fragments - genetics</subject><subject>Peptide Fragments - immunology</subject><subject>polyclonal antibodies</subject><subject>proteins</subject><subject>Proteomics - methods</subject><subject>Quality Control</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - immunology</subject><subject>surveys</subject><subject>Tissue-independent mitochondrial protein</subject><subject>tissues</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtLxDAQh4Mouj7unjQ3T10nyTZtvYn4AsGDj2tIk8maZdusSav435tl1ZswEBi--WXmI-SYwZQBk-eLqW6nHBib5gJWbpEJg0YWIKDZJhMAEAWXTbVH9lNaQAZnpdwle5yzqm6YmJDXS9p5E8Mq4kpHPfjQ0-BybwjmLfQ2ek1dDB01uFwmOibfz2mn5z0O3tAWtU300w9v1Hfd2AftnO_98HVIdpxeJjz6eQ_Iy83189Vd8fB4e391-VAYUYmhsCAaU3JpuOaAs0rYthLI69I6IXIbgMsamnwTstJVoq54breMG6tR1404IGeb3FUM7yOmQXU-rVfVPYYxqYbJksOM8UzChszHphTRqVX0nY5fioFay1QLpVu1lqlyZZl55OQnfGw7tH8Dv_YycLoBnA5Kz6NP6uUpJ8gsHmRdQiYuNgRmCR8eo0rGY2_Q-ohmUDb4____BoLPjJo</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Ru, Yawei</creator><creator>Yin, Liang</creator><creator>Sun, Haidan</creator><creator>Yin, Songyue</creator><creator>Pan, Qin</creator><creator>Wei, Hanfu</creator><creator>Wu, Lin</creator><creator>Liu, Siqi</creator><general>Elsevier Inc</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>20120201</creationdate><title>A micropreparation of mitochondria from cells using magnetic beads with immunoaffinity</title><author>Ru, Yawei ; Yin, Liang ; Sun, Haidan ; Yin, Songyue ; Pan, Qin ; Wei, Hanfu ; Wu, Lin ; Liu, Siqi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-d039c526c2a20e473db73e285df3326c0026809109e15f73872326b12cdaea893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adaptor Proteins, Signal Transducing - genetics</topic><topic>Adaptor Proteins, Signal Transducing - immunology</topic><topic>Animals</topic><topic>Antibody Affinity</topic><topic>Base Sequence</topic><topic>Cell Fractionation - methods</topic><topic>Cell Fractionation - standards</topic><topic>Cell Line</topic><topic>cultured cells</topic><topic>Cytochrome b5 type B (CYB5B)</topic><topic>Cytochromes b5 - genetics</topic><topic>Cytochromes b5 - immunology</topic><topic>DNA Primers - genetics</topic><topic>Immunomagnetic beads</topic><topic>Immunomagnetic Separation - methods</topic><topic>Immunomagnetic Separation - standards</topic><topic>liver</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - immunology</topic><topic>Mice</topic><topic>mitochondria</topic><topic>Mitochondria - chemistry</topic><topic>Mitochondria - immunology</topic><topic>Mitochondria isolation</topic><topic>mitochondrial membrane</topic><topic>Peptide Fragments - genetics</topic><topic>Peptide Fragments - immunology</topic><topic>polyclonal antibodies</topic><topic>proteins</topic><topic>Proteomics - methods</topic><topic>Quality Control</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - immunology</topic><topic>surveys</topic><topic>Tissue-independent mitochondrial protein</topic><topic>tissues</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ru, Yawei</creatorcontrib><creatorcontrib>Yin, Liang</creatorcontrib><creatorcontrib>Sun, Haidan</creatorcontrib><creatorcontrib>Yin, Songyue</creatorcontrib><creatorcontrib>Pan, Qin</creatorcontrib><creatorcontrib>Wei, Hanfu</creatorcontrib><creatorcontrib>Wu, Lin</creatorcontrib><creatorcontrib>Liu, Siqi</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>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ru, Yawei</au><au>Yin, Liang</au><au>Sun, Haidan</au><au>Yin, Songyue</au><au>Pan, Qin</au><au>Wei, Hanfu</au><au>Wu, Lin</au><au>Liu, Siqi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A micropreparation of mitochondria from cells using magnetic beads with immunoaffinity</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>421</volume><issue>1</issue><spage>219</spage><epage>226</epage><pages>219-226</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>Mitochondrial preparation is a key technique in the study of mitochondria. Growing evidence has demonstrated that mitochondrial proteins are tissue or cell type dependent. Locating the proteins in the global presence of mitochondrial membranes is a primary consideration in adopting antibodies for affinity enrichment of mitochondria on a micro scale. Two proteins located on the outer membrane of mitochondria, cytochrome b5 type B (CYB5B) and synaptojanin-2-binding protein (SYNJ2BP), were selected as candidates based on a survey of databases and the literature. The polyclonal antibodies against the truncated CYB5B and SYNJ2BP exhibited specific recognition to mitochondria and wider sensitivity to several tested mouse tissues and cell lines, whereas the antibody 22-kDa translocase of the outer mitochondrial membrane (TOM22) nearly missed detection of mitochondria in the liver and responded minimally to mitochondria from H9C2 and L-02 cells. Through the affinity enrichment for cellular mitochondria using magnetic beads coated with anti-CYB5B or anti-SYNJ2BP, we found that the anti-CYB5B beads could enrich mitochondria more efficiently even on a scale of 10,000 cultured cells. For the integrity and protein components, the enriched mitochondria on anti-CYB5B were carefully examined and were accepted in further functional study. We propose that an anti-CYB5B immunomagnetic approach is feasible in the micropreparation of mitochondria from cultured cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22178913</pmid><doi>10.1016/j.ab.2011.11.015</doi><tpages>8</tpages></addata></record> |
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subjects | Adaptor Proteins, Signal Transducing - genetics Adaptor Proteins, Signal Transducing - immunology Animals Antibody Affinity Base Sequence Cell Fractionation - methods Cell Fractionation - standards Cell Line cultured cells Cytochrome b5 type B (CYB5B) Cytochromes b5 - genetics Cytochromes b5 - immunology DNA Primers - genetics Immunomagnetic beads Immunomagnetic Separation - methods Immunomagnetic Separation - standards liver Membrane Proteins - genetics Membrane Proteins - immunology Mice mitochondria Mitochondria - chemistry Mitochondria - immunology Mitochondria isolation mitochondrial membrane Peptide Fragments - genetics Peptide Fragments - immunology polyclonal antibodies proteins Proteomics - methods Quality Control Recombinant Proteins - genetics Recombinant Proteins - immunology surveys Tissue-independent mitochondrial protein tissues |
title | A micropreparation of mitochondria from cells using magnetic beads with immunoaffinity |
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