Cell chip array for microfluidic proteomics enabling rapid in situ assessment of intracellular protein phosphorylation
We discuss the ability to perform fluorescent immunocytochemistry, following cell fixation, using a microfluidic array of primary, nonadherent, single CD 34 + stem cells. The technique requires small cell samples and proceeds with no cell loss, making it well-suited to monitoring these rare patient-...
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Veröffentlicht in: | Biomicrofluidics 2011-06, Vol.5 (2), p.024106-024106-7 |
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creator | Faley, Shannon L. Copland, Mhairi Reboud, Julien Cooper, Jonathan M. |
description | We discuss the ability to perform fluorescent immunocytochemistry, following cell fixation, using a microfluidic array of primary, nonadherent, single
CD
34
+
stem cells. The technique requires small cell samples and proceeds with no cell loss, making it well-suited to monitoring these rare patient-derived cells. The chip allows us to correlate live cell dynamics across arrays of individual cells with post-translational modifications of intracellular proteins, following their exposure to drug treatments. Results also show that due to the microfluidic environment, the time scale of cell fixation was significantly reduced compared to conventional methods, leading to greater confidence in the status of the protein modifications studied. |
doi_str_mv | 10.1063/1.3587095 |
format | Article |
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CD
34
+
stem cells. The technique requires small cell samples and proceeds with no cell loss, making it well-suited to monitoring these rare patient-derived cells. The chip allows us to correlate live cell dynamics across arrays of individual cells with post-translational modifications of intracellular proteins, following their exposure to drug treatments. Results also show that due to the microfluidic environment, the time scale of cell fixation was significantly reduced compared to conventional methods, leading to greater confidence in the status of the protein modifications studied.</description><identifier>ISSN: 1932-1058</identifier><identifier>EISSN: 1932-1058</identifier><identifier>DOI: 10.1063/1.3587095</identifier><identifier>PMID: 21673844</identifier><identifier>CODEN: BIOMGB</identifier><language>eng</language><publisher>United States: American Institute of Physics</publisher><subject>Regular</subject><ispartof>Biomicrofluidics, 2011-06, Vol.5 (2), p.024106-024106-7</ispartof><rights>American Institute of Physics</rights><rights>2011 American Institute of Physics</rights><rights>Copyright © 2011 American Institute of Physics 2011 American Institute of Physics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-54abe04801a0e3b7ef83aeb25a3cdddde5fee1a4bcc0db47204280c0b39f97993</citedby><cites>FETCH-LOGICAL-c498t-54abe04801a0e3b7ef83aeb25a3cdddde5fee1a4bcc0db47204280c0b39f97993</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/PMC3112183/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://pubs.aip.org/bmf/article-lookup/doi/10.1063/1.3587095$$EHTML$$P50$$Gscitation$$H</linktohtml><link.rule.ids>230,314,724,777,781,791,882,4498,27905,27906,53772,53774,76133</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21673844$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Faley, Shannon L.</creatorcontrib><creatorcontrib>Copland, Mhairi</creatorcontrib><creatorcontrib>Reboud, Julien</creatorcontrib><creatorcontrib>Cooper, Jonathan M.</creatorcontrib><title>Cell chip array for microfluidic proteomics enabling rapid in situ assessment of intracellular protein phosphorylation</title><title>Biomicrofluidics</title><addtitle>Biomicrofluidics</addtitle><description>We discuss the ability to perform fluorescent immunocytochemistry, following cell fixation, using a microfluidic array of primary, nonadherent, single
CD
34
+
stem cells. The technique requires small cell samples and proceeds with no cell loss, making it well-suited to monitoring these rare patient-derived cells. The chip allows us to correlate live cell dynamics across arrays of individual cells with post-translational modifications of intracellular proteins, following their exposure to drug treatments. Results also show that due to the microfluidic environment, the time scale of cell fixation was significantly reduced compared to conventional methods, leading to greater confidence in the status of the protein modifications studied.</description><subject>Regular</subject><issn>1932-1058</issn><issn>1932-1058</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kUtr3DAUhUVoyKtd9A8U7UoCk-hhj-VFC2FI0kAgm3YtruWrjIptuZI9MP--cmYymVISgZC4-s7RlQ4hnzm75Gwur_ilzFXByvyAnPBSihlnufqwtz8mpzH-ZiznhRBH5FjweSFVlp2Q1QKbhpql6ymEAGtqfaCtM8HbZnS1M7QPfkCfSpFiB1XjuicaoHc1dR2NbhgpxIgxttgN1NtUHQKY5Do2EDbqBPZLH9MM6wYG57uP5NBCE_HTdj0jv25vfi5-zB4e7-4X1w8zk5VqmOUZVMgyxTgwlFWBVknASuQgTZ0G5haRQ1YZw-oqKwTLhGKGVbK0ZVGW8ox83_j2Y9VibXBqrtF9cC2Etfbg9L8nnVvqJ7_SknPBlUwGX7cGwf8ZMQ66dXF6HXTox6hVIbiYl8VEnm_I9HcxBrS7WzjTU0ya621Mif2y39aOfMklAd82QDRueP6xt92mBPWUoH5OUKcEk_7iLf3Kh1et7mv7Hvx_638BTozDmQ</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>Faley, Shannon L.</creator><creator>Copland, Mhairi</creator><creator>Reboud, Julien</creator><creator>Cooper, Jonathan M.</creator><general>American Institute of Physics</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110601</creationdate><title>Cell chip array for microfluidic proteomics enabling rapid in situ assessment of intracellular protein phosphorylation</title><author>Faley, Shannon L. ; Copland, Mhairi ; Reboud, Julien ; Cooper, Jonathan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-54abe04801a0e3b7ef83aeb25a3cdddde5fee1a4bcc0db47204280c0b39f97993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Regular</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Faley, Shannon L.</creatorcontrib><creatorcontrib>Copland, Mhairi</creatorcontrib><creatorcontrib>Reboud, Julien</creatorcontrib><creatorcontrib>Cooper, Jonathan M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biomicrofluidics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Faley, Shannon L.</au><au>Copland, Mhairi</au><au>Reboud, Julien</au><au>Cooper, Jonathan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell chip array for microfluidic proteomics enabling rapid in situ assessment of intracellular protein phosphorylation</atitle><jtitle>Biomicrofluidics</jtitle><addtitle>Biomicrofluidics</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>5</volume><issue>2</issue><spage>024106</spage><epage>024106-7</epage><pages>024106-024106-7</pages><issn>1932-1058</issn><eissn>1932-1058</eissn><coden>BIOMGB</coden><abstract>We discuss the ability to perform fluorescent immunocytochemistry, following cell fixation, using a microfluidic array of primary, nonadherent, single
CD
34
+
stem cells. The technique requires small cell samples and proceeds with no cell loss, making it well-suited to monitoring these rare patient-derived cells. The chip allows us to correlate live cell dynamics across arrays of individual cells with post-translational modifications of intracellular proteins, following their exposure to drug treatments. Results also show that due to the microfluidic environment, the time scale of cell fixation was significantly reduced compared to conventional methods, leading to greater confidence in the status of the protein modifications studied.</abstract><cop>United States</cop><pub>American Institute of Physics</pub><pmid>21673844</pmid><doi>10.1063/1.3587095</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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title | Cell chip array for microfluidic proteomics enabling rapid in situ assessment of intracellular protein phosphorylation |
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