Adhesion of Antibody-Functionalized Polymersomes
Polymersomes are vesicles made from synthetic block copolymers. The adhesiveness of micron-sized polymersomes, functionalized with antibodies that bind to vascular cell adhesion molecules, which could be useful for vascular targeting, was measured. Intercellular adhesion molecule-1 (ICAM-1) is an en...
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Veröffentlicht in: | Langmuir 2006-04, Vol.22 (9), p.3975-3979 |
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description | Polymersomes are vesicles made from synthetic block copolymers. The adhesiveness of micron-sized polymersomes, functionalized with antibodies that bind to vascular cell adhesion molecules, which could be useful for vascular targeting, was measured. Intercellular adhesion molecule-1 (ICAM-1) is an endothelial cell adhesion molecule whose expression increases during inflammatory disease, and is therefore a natural target for vascular delivery. We functionalized polymersomes with an anti-ICAM-1 antibody, using modular biotin−avidin chemistry. Micropipet aspiration was used to confirm specific adhesion and measure the adhesion strength between an anti-ICAM-1-coated polymersome and an ICAM-1-coated polystyrene microsphere at various surface densities of adhesion molecules. The adhesion is kinetically trapped, and adhesion strength is quantified by the critical tension for detachment. The adhesion strength increases in proportion to the surface density of anti-ICAM-1 molecules, in contrast to results seen previously when measuring adhesion between biotinylated vesicles and avidin-coated beads (Lin et al. Langmuir 2004, 20, 5493). The difference in dependence on the density of functional groups is likely due to the molecular presentation at the vesicle surface; in the current study, the presentation of biotinylated anti-ICAM-1 on a layer of avidin leads to the effective presentation of the anti-ICAM-1 and, thus, a monotonic increase in adhesiveness with antibody density. |
doi_str_mv | 10.1021/la052445c |
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Peter ; Zhang, Ying ; Hammer, Daniel A</creator><creatorcontrib>Lin, John J ; Ghoroghchian, P. Peter ; Zhang, Ying ; Hammer, Daniel A</creatorcontrib><description>Polymersomes are vesicles made from synthetic block copolymers. The adhesiveness of micron-sized polymersomes, functionalized with antibodies that bind to vascular cell adhesion molecules, which could be useful for vascular targeting, was measured. Intercellular adhesion molecule-1 (ICAM-1) is an endothelial cell adhesion molecule whose expression increases during inflammatory disease, and is therefore a natural target for vascular delivery. We functionalized polymersomes with an anti-ICAM-1 antibody, using modular biotin−avidin chemistry. Micropipet aspiration was used to confirm specific adhesion and measure the adhesion strength between an anti-ICAM-1-coated polymersome and an ICAM-1-coated polystyrene microsphere at various surface densities of adhesion molecules. The adhesion is kinetically trapped, and adhesion strength is quantified by the critical tension for detachment. The adhesion strength increases in proportion to the surface density of anti-ICAM-1 molecules, in contrast to results seen previously when measuring adhesion between biotinylated vesicles and avidin-coated beads (Lin et al. Langmuir 2004, 20, 5493). The difference in dependence on the density of functional groups is likely due to the molecular presentation at the vesicle surface; in the current study, the presentation of biotinylated anti-ICAM-1 on a layer of avidin leads to the effective presentation of the anti-ICAM-1 and, thus, a monotonic increase in adhesiveness with antibody density.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la052445c</identifier><identifier>PMID: 16618135</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Adhesiveness ; Animals ; Antibodies - chemistry ; Avidin - chemistry ; Biopolymers - chemistry ; Biotin - chemistry ; Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; Fluorescent Dyes ; General and physical chemistry ; Humans ; In Vitro Techniques ; Intercellular Adhesion Molecule-1 - chemistry ; Intercellular Adhesion Molecule-1 - immunology ; Membranes ; Microspheres ; Multiprotein Complexes - chemistry ; Polystyrenes - chemistry ; Surface Properties</subject><ispartof>Langmuir, 2006-04, Vol.22 (9), p.3975-3979</ispartof><rights>Copyright © 2006 American Chemical Society</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-7b0c30344a7065ac06575436fa4c160ac350dc06ab8c2d4034d6eb2a119290813</citedby><cites>FETCH-LOGICAL-a381t-7b0c30344a7065ac06575436fa4c160ac350dc06ab8c2d4034d6eb2a119290813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/la052445c$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la052445c$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27081,27929,27930,56743,56793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17708024$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16618135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, John J</creatorcontrib><creatorcontrib>Ghoroghchian, P. Peter</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Hammer, Daniel A</creatorcontrib><title>Adhesion of Antibody-Functionalized Polymersomes</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Polymersomes are vesicles made from synthetic block copolymers. The adhesiveness of micron-sized polymersomes, functionalized with antibodies that bind to vascular cell adhesion molecules, which could be useful for vascular targeting, was measured. Intercellular adhesion molecule-1 (ICAM-1) is an endothelial cell adhesion molecule whose expression increases during inflammatory disease, and is therefore a natural target for vascular delivery. We functionalized polymersomes with an anti-ICAM-1 antibody, using modular biotin−avidin chemistry. Micropipet aspiration was used to confirm specific adhesion and measure the adhesion strength between an anti-ICAM-1-coated polymersome and an ICAM-1-coated polystyrene microsphere at various surface densities of adhesion molecules. The adhesion is kinetically trapped, and adhesion strength is quantified by the critical tension for detachment. The adhesion strength increases in proportion to the surface density of anti-ICAM-1 molecules, in contrast to results seen previously when measuring adhesion between biotinylated vesicles and avidin-coated beads (Lin et al. Langmuir 2004, 20, 5493). The difference in dependence on the density of functional groups is likely due to the molecular presentation at the vesicle surface; in the current study, the presentation of biotinylated anti-ICAM-1 on a layer of avidin leads to the effective presentation of the anti-ICAM-1 and, thus, a monotonic increase in adhesiveness with antibody density.</description><subject>Adhesiveness</subject><subject>Animals</subject><subject>Antibodies - chemistry</subject><subject>Avidin - chemistry</subject><subject>Biopolymers - chemistry</subject><subject>Biotin - chemistry</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Exact sciences and technology</subject><subject>Fluorescent Dyes</subject><subject>General and physical chemistry</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Intercellular Adhesion Molecule-1 - chemistry</subject><subject>Intercellular Adhesion Molecule-1 - immunology</subject><subject>Membranes</subject><subject>Microspheres</subject><subject>Multiprotein Complexes - chemistry</subject><subject>Polystyrenes - chemistry</subject><subject>Surface Properties</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0M9LwzAUB_AgipvTg_-A7KLgofrSJE17HMP5g4EDJ3gLr2mKnW2jSQvOv97IxnbxksB7Hx5fvoScU7ihENPbGkHEnAt9QIZUxBCJNJaHZAiSs0jyhA3IifcrAMgYz47JgCYJTSkTQwKT4t34yrZjW44nbVfltlhHs77VXRhiXf2YYryw9boxztvG-FNyVGLtzdn2H5HX2d1y-hDNn-8fp5N5hCylXSRz0AwY5yghEajDIwVnSYlc0wRQMwFFmGKe6rjgQRaJyWOkNIszCNlG5Gpz99PZr974TjWV16ausTW29yqRqWQZTQO83kDtrPfOlOrTVQ26taKg_upRu3qCvdge7fPGFHu57SOAyy1Ar7EuHba68nsnJaQQ8-Cijat8Z753e3QfIRiTQi0XL-ppyufwJjP1tL-L2quV7V2o1v8T8BdadIWj</recordid><startdate>20060425</startdate><enddate>20060425</enddate><creator>Lin, John J</creator><creator>Ghoroghchian, P. Peter</creator><creator>Zhang, Ying</creator><creator>Hammer, Daniel A</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>7X8</scope></search><sort><creationdate>20060425</creationdate><title>Adhesion of Antibody-Functionalized Polymersomes</title><author>Lin, John J ; Ghoroghchian, P. Peter ; Zhang, Ying ; Hammer, Daniel A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-7b0c30344a7065ac06575436fa4c160ac350dc06ab8c2d4034d6eb2a119290813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adhesiveness</topic><topic>Animals</topic><topic>Antibodies - chemistry</topic><topic>Avidin - chemistry</topic><topic>Biopolymers - chemistry</topic><topic>Biotin - chemistry</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Exact sciences and technology</topic><topic>Fluorescent Dyes</topic><topic>General and physical chemistry</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Intercellular Adhesion Molecule-1 - chemistry</topic><topic>Intercellular Adhesion Molecule-1 - immunology</topic><topic>Membranes</topic><topic>Microspheres</topic><topic>Multiprotein Complexes - chemistry</topic><topic>Polystyrenes - chemistry</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, John J</creatorcontrib><creatorcontrib>Ghoroghchian, P. Peter</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Hammer, Daniel A</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>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, John J</au><au>Ghoroghchian, P. Peter</au><au>Zhang, Ying</au><au>Hammer, Daniel A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adhesion of Antibody-Functionalized Polymersomes</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2006-04-25</date><risdate>2006</risdate><volume>22</volume><issue>9</issue><spage>3975</spage><epage>3979</epage><pages>3975-3979</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>Polymersomes are vesicles made from synthetic block copolymers. The adhesiveness of micron-sized polymersomes, functionalized with antibodies that bind to vascular cell adhesion molecules, which could be useful for vascular targeting, was measured. Intercellular adhesion molecule-1 (ICAM-1) is an endothelial cell adhesion molecule whose expression increases during inflammatory disease, and is therefore a natural target for vascular delivery. We functionalized polymersomes with an anti-ICAM-1 antibody, using modular biotin−avidin chemistry. Micropipet aspiration was used to confirm specific adhesion and measure the adhesion strength between an anti-ICAM-1-coated polymersome and an ICAM-1-coated polystyrene microsphere at various surface densities of adhesion molecules. The adhesion is kinetically trapped, and adhesion strength is quantified by the critical tension for detachment. The adhesion strength increases in proportion to the surface density of anti-ICAM-1 molecules, in contrast to results seen previously when measuring adhesion between biotinylated vesicles and avidin-coated beads (Lin et al. Langmuir 2004, 20, 5493). The difference in dependence on the density of functional groups is likely due to the molecular presentation at the vesicle surface; in the current study, the presentation of biotinylated anti-ICAM-1 on a layer of avidin leads to the effective presentation of the anti-ICAM-1 and, thus, a monotonic increase in adhesiveness with antibody density.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16618135</pmid><doi>10.1021/la052445c</doi><tpages>5</tpages></addata></record> |
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subjects | Adhesiveness Animals Antibodies - chemistry Avidin - chemistry Biopolymers - chemistry Biotin - chemistry Chemistry Colloidal state and disperse state Exact sciences and technology Fluorescent Dyes General and physical chemistry Humans In Vitro Techniques Intercellular Adhesion Molecule-1 - chemistry Intercellular Adhesion Molecule-1 - immunology Membranes Microspheres Multiprotein Complexes - chemistry Polystyrenes - chemistry Surface Properties |
title | Adhesion of Antibody-Functionalized Polymersomes |
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