Capture of Rare Cells in Suspension with Antibody-Coated Polystyrene Beads
A method for the separation of one cell type present in small number from a predominant mixture of cell types using macroscopic polystyrene beads is demonstrated. An antibody specific to murine leukocytes (CD45) was adsorbed to the surface of the beads. Beads and murine hybridoma B cells were placed...
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Veröffentlicht in: | Biotechnology progress 1999-03, Vol.15 (2), p.238-244 |
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creator | Gomez, Shawn M. Choy, Garry Kabir, Norman Leonard, Edward F. |
description | A method for the separation of one cell type present in small number from a predominant mixture of cell types using macroscopic polystyrene beads is demonstrated. An antibody specific to murine leukocytes (CD45) was adsorbed to the surface of the beads. Beads and murine hybridoma B cells were placed in test tubes and periodically inverted at fixed time intervals, causing the beads to settle through the suspension under creeping flow conditions. Capture was dependent upon interception: the captured cells must have traveled along streamlines that brought them to within a cell radius of the bead surface. B cells attached to 99‐μm beads (maximum shear rate 8.1 s−1) were captured with greater efficiency but in lesser quantity than those attached to 170‐μm beads (maximum shear rate 13.9 s−1). Cell capture unexpectedly reached a plateau in less than 2 h, a phenomenon that appears to involve changes in both the cells and the beads. Capture of cells was effective out to dilutions of 1:10 000 with purity in the captured population of better than 74%. This method allows for the study of physical parameters important for cell attachment and capture as well as for practical separation of rare cells. |
doi_str_mv | 10.1021/bp990001z |
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An antibody specific to murine leukocytes (CD45) was adsorbed to the surface of the beads. Beads and murine hybridoma B cells were placed in test tubes and periodically inverted at fixed time intervals, causing the beads to settle through the suspension under creeping flow conditions. Capture was dependent upon interception: the captured cells must have traveled along streamlines that brought them to within a cell radius of the bead surface. B cells attached to 99‐μm beads (maximum shear rate 8.1 s−1) were captured with greater efficiency but in lesser quantity than those attached to 170‐μm beads (maximum shear rate 13.9 s−1). Cell capture unexpectedly reached a plateau in less than 2 h, a phenomenon that appears to involve changes in both the cells and the beads. Capture of cells was effective out to dilutions of 1:10 000 with purity in the captured population of better than 74%. This method allows for the study of physical parameters important for cell attachment and capture as well as for practical separation of rare cells.</description><identifier>ISSN: 8756-7938</identifier><identifier>EISSN: 1520-6033</identifier><identifier>DOI: 10.1021/bp990001z</identifier><identifier>PMID: 10194399</identifier><identifier>CODEN: BIPRET</identifier><language>eng</language><publisher>USA: American Chemical Society</publisher><subject>Adsorption ; Animals ; Antibodies ; Antibodies - metabolism ; B-Lymphocytes - cytology ; B-Lymphocytes - immunology ; Biological and medical sciences ; Biotechnology ; Cell Separation - methods ; Coated materials ; Coated Materials, Biocompatible ; Diverse techniques ; Fundamental and applied biological sciences. Psychology ; Hybridomas - cytology ; Hybridomas - metabolism ; Leukocyte Common Antigens - immunology ; Methods. Procedures. Technologies ; Mice ; Microspheres ; Molecular and cellular biology ; Osmolar Concentration ; Others ; Polystyrenes ; Suspensions ; Suspensions (fluids) ; Time Factors ; Various methods and equipments</subject><ispartof>Biotechnology progress, 1999-03, Vol.15 (2), p.238-244</ispartof><rights>Copyright © 1999 American Institute of Chemical Engineers (AIChE)</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4521-52da3ac6c792cf38573a1770b66b84c41f14d1a1d0948bfdb47e50da68fd40583</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1021%2Fbp990001z$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1021%2Fbp990001z$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1797658$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10194399$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomez, Shawn M.</creatorcontrib><creatorcontrib>Choy, Garry</creatorcontrib><creatorcontrib>Kabir, Norman</creatorcontrib><creatorcontrib>Leonard, Edward F.</creatorcontrib><title>Capture of Rare Cells in Suspension with Antibody-Coated Polystyrene Beads</title><title>Biotechnology progress</title><addtitle>Biotechnol Progress</addtitle><description>A method for the separation of one cell type present in small number from a predominant mixture of cell types using macroscopic polystyrene beads is demonstrated. An antibody specific to murine leukocytes (CD45) was adsorbed to the surface of the beads. Beads and murine hybridoma B cells were placed in test tubes and periodically inverted at fixed time intervals, causing the beads to settle through the suspension under creeping flow conditions. Capture was dependent upon interception: the captured cells must have traveled along streamlines that brought them to within a cell radius of the bead surface. B cells attached to 99‐μm beads (maximum shear rate 8.1 s−1) were captured with greater efficiency but in lesser quantity than those attached to 170‐μm beads (maximum shear rate 13.9 s−1). Cell capture unexpectedly reached a plateau in less than 2 h, a phenomenon that appears to involve changes in both the cells and the beads. Capture of cells was effective out to dilutions of 1:10 000 with purity in the captured population of better than 74%. This method allows for the study of physical parameters important for cell attachment and capture as well as for practical separation of rare cells.</description><subject>Adsorption</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies - metabolism</subject><subject>B-Lymphocytes - cytology</subject><subject>B-Lymphocytes - immunology</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell Separation - methods</subject><subject>Coated materials</subject><subject>Coated Materials, Biocompatible</subject><subject>Diverse techniques</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hybridomas - cytology</subject><subject>Hybridomas - metabolism</subject><subject>Leukocyte Common Antigens - immunology</subject><subject>Methods. Procedures. Technologies</subject><subject>Mice</subject><subject>Microspheres</subject><subject>Molecular and cellular biology</subject><subject>Osmolar Concentration</subject><subject>Others</subject><subject>Polystyrenes</subject><subject>Suspensions</subject><subject>Suspensions (fluids)</subject><subject>Time Factors</subject><subject>Various methods and equipments</subject><issn>8756-7938</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0ctu1TAQBmALUdHTwoIXQFkgpC5Cfb8s26hNW1XlqBfBznJsRxhykmAnKuHpSZujwqbqarz4_rHHA8B7BD8jiNFh1SsFIUR_XoEVYhjmHBLyGqykYDwXishdsJfSj5lIyPEbsIsgUpQotQIXhemHMfqsq7NrM9fCN03KQpvdjKn3bQpdm92H4Xt21A6h6tyUF50ZvMvWXTOlYYq-9dmxNy69BTu1aZJ_t6374O705LY4yy-_lOfF0WVuKcMoZ9gZYiy3QmFbE8kEMUgIWHFeSWopqhF1yCAHFZVV7SoqPIPOcFk7Cpkk--DT0reP3a_Rp0FvQrLzs03ruzFprrjEs3wRYvTQT_AXIRIYMyLoDA8WaGOXUvS17mPYmDhpBPXDKvTTKmb7Ydt0rDbe_SeXv5_Bxy0wyZqmjqa1If1zQgn-OC5a2H1o_PT8hfr4dn29nOdMvmRCGvzvp4yJPzUXRDD99arU5bey5GusNCR_AbFprUg</recordid><startdate>19990301</startdate><enddate>19990301</enddate><creator>Gomez, Shawn M.</creator><creator>Choy, Garry</creator><creator>Kabir, Norman</creator><creator>Leonard, Edward F.</creator><general>American Chemical Society</general><general>American Institute of Chemical Engineers</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19990301</creationdate><title>Capture of Rare Cells in Suspension with Antibody-Coated Polystyrene Beads</title><author>Gomez, Shawn M. ; Choy, Garry ; Kabir, Norman ; Leonard, Edward F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4521-52da3ac6c792cf38573a1770b66b84c41f14d1a1d0948bfdb47e50da68fd40583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adsorption</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies - metabolism</topic><topic>B-Lymphocytes - cytology</topic><topic>B-Lymphocytes - immunology</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell Separation - methods</topic><topic>Coated materials</topic><topic>Coated Materials, Biocompatible</topic><topic>Diverse techniques</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hybridomas - cytology</topic><topic>Hybridomas - metabolism</topic><topic>Leukocyte Common Antigens - immunology</topic><topic>Methods. Procedures. Technologies</topic><topic>Mice</topic><topic>Microspheres</topic><topic>Molecular and cellular biology</topic><topic>Osmolar Concentration</topic><topic>Others</topic><topic>Polystyrenes</topic><topic>Suspensions</topic><topic>Suspensions (fluids)</topic><topic>Time Factors</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomez, Shawn M.</creatorcontrib><creatorcontrib>Choy, Garry</creatorcontrib><creatorcontrib>Kabir, Norman</creatorcontrib><creatorcontrib>Leonard, Edward F.</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology progress</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomez, Shawn M.</au><au>Choy, Garry</au><au>Kabir, Norman</au><au>Leonard, Edward F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Capture of Rare Cells in Suspension with Antibody-Coated Polystyrene Beads</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Progress</addtitle><date>1999-03-01</date><risdate>1999</risdate><volume>15</volume><issue>2</issue><spage>238</spage><epage>244</epage><pages>238-244</pages><issn>8756-7938</issn><eissn>1520-6033</eissn><coden>BIPRET</coden><abstract>A method for the separation of one cell type present in small number from a predominant mixture of cell types using macroscopic polystyrene beads is demonstrated. An antibody specific to murine leukocytes (CD45) was adsorbed to the surface of the beads. Beads and murine hybridoma B cells were placed in test tubes and periodically inverted at fixed time intervals, causing the beads to settle through the suspension under creeping flow conditions. Capture was dependent upon interception: the captured cells must have traveled along streamlines that brought them to within a cell radius of the bead surface. B cells attached to 99‐μm beads (maximum shear rate 8.1 s−1) were captured with greater efficiency but in lesser quantity than those attached to 170‐μm beads (maximum shear rate 13.9 s−1). Cell capture unexpectedly reached a plateau in less than 2 h, a phenomenon that appears to involve changes in both the cells and the beads. Capture of cells was effective out to dilutions of 1:10 000 with purity in the captured population of better than 74%. This method allows for the study of physical parameters important for cell attachment and capture as well as for practical separation of rare cells.</abstract><cop>USA</cop><pub>American Chemical Society</pub><pmid>10194399</pmid><doi>10.1021/bp990001z</doi><tpages>7</tpages></addata></record> |
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subjects | Adsorption Animals Antibodies Antibodies - metabolism B-Lymphocytes - cytology B-Lymphocytes - immunology Biological and medical sciences Biotechnology Cell Separation - methods Coated materials Coated Materials, Biocompatible Diverse techniques Fundamental and applied biological sciences. Psychology Hybridomas - cytology Hybridomas - metabolism Leukocyte Common Antigens - immunology Methods. Procedures. Technologies Mice Microspheres Molecular and cellular biology Osmolar Concentration Others Polystyrenes Suspensions Suspensions (fluids) Time Factors Various methods and equipments |
title | Capture of Rare Cells in Suspension with Antibody-Coated Polystyrene Beads |
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