Multitasking by Multivalent Circular DNA Aptamers
Nucleic acid aptamers are finding increasing applications in biology, especially as therapeutic candidates and diagnostic components. An important characteristic in meeting the needs of these applications is improved stability in physiological fluids, which is most often accomplished with chemical m...
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Veröffentlicht in: | Chembiochem : a European journal of chemical biology 2006-03, Vol.7 (3), p.535-544 |
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creator | Di Giusto, Daniel A Knox, Sarah M Lai, Yuching Tyrelle, Gregory D Aung, May T King, Garry C |
description | Nucleic acid aptamers are finding increasing applications in biology, especially as therapeutic candidates and diagnostic components. An important characteristic in meeting the needs of these applications is improved stability in physiological fluids, which is most often accomplished with chemical modification or unnatural nucleotides. In an alternative approach we have specified the design of a multivalent circular DNA aptamer topology that encompasses a number of properties relevant to nucleic acid therapeutic candidates, especially the ability to multitask by combining different activities together within a modular structure. Improved stability in blood products, greater conformational stability, antidoting by complementary circular antiaptamers, heterovalency, transcription factor decoy activity and minimal unintended effects upon the cellular innate immune response are desirable properties that are described here. Multitasking by circular DNA aptamers could similarly find applications in diagnostics and biomaterials, where the combination of interchangeable modules might generate new functions, such as anticoagulation coupled with reversible cell capture as, described here. These results provide a platform for further exploration of multivalent circular aptamer properties, especially in novel combinations of nucleic acid therapeutic modes. |
doi_str_mv | 10.1002/cbic.200500316 |
format | Article |
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An important characteristic in meeting the needs of these applications is improved stability in physiological fluids, which is most often accomplished with chemical modification or unnatural nucleotides. In an alternative approach we have specified the design of a multivalent circular DNA aptamer topology that encompasses a number of properties relevant to nucleic acid therapeutic candidates, especially the ability to multitask by combining different activities together within a modular structure. Improved stability in blood products, greater conformational stability, antidoting by complementary circular antiaptamers, heterovalency, transcription factor decoy activity and minimal unintended effects upon the cellular innate immune response are desirable properties that are described here. Multitasking by circular DNA aptamers could similarly find applications in diagnostics and biomaterials, where the combination of interchangeable modules might generate new functions, such as anticoagulation coupled with reversible cell capture as, described here. These results provide a platform for further exploration of multivalent circular aptamer properties, especially in novel combinations of nucleic acid therapeutic modes.</description><identifier>ISSN: 1439-4227</identifier><identifier>EISSN: 1439-7633</identifier><identifier>DOI: 10.1002/cbic.200500316</identifier><identifier>PMID: 16482500</identifier><language>eng</language><publisher>Weinheim: Wiley-VCH Verlag</publisher><subject>Aptamers, Nucleotide - chemistry ; Cell Separation ; Cells, Cultured ; DNA structures ; DNA, Circular - chemistry ; Flow Cytometry ; Humans ; immobilization ; nanostructures ; nucleic acids ; therapeutic targeting</subject><ispartof>Chembiochem : a European journal of chemical biology, 2006-03, Vol.7 (3), p.535-544</ispartof><rights>Copyright © 2006 WILEY‐VCH Verlag GmbH & Co. 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An important characteristic in meeting the needs of these applications is improved stability in physiological fluids, which is most often accomplished with chemical modification or unnatural nucleotides. In an alternative approach we have specified the design of a multivalent circular DNA aptamer topology that encompasses a number of properties relevant to nucleic acid therapeutic candidates, especially the ability to multitask by combining different activities together within a modular structure. Improved stability in blood products, greater conformational stability, antidoting by complementary circular antiaptamers, heterovalency, transcription factor decoy activity and minimal unintended effects upon the cellular innate immune response are desirable properties that are described here. Multitasking by circular DNA aptamers could similarly find applications in diagnostics and biomaterials, where the combination of interchangeable modules might generate new functions, such as anticoagulation coupled with reversible cell capture as, described here. These results provide a platform for further exploration of multivalent circular aptamer properties, especially in novel combinations of nucleic acid therapeutic modes.</description><subject>Aptamers, Nucleotide - chemistry</subject><subject>Cell Separation</subject><subject>Cells, Cultured</subject><subject>DNA structures</subject><subject>DNA, Circular - chemistry</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>immobilization</subject><subject>nanostructures</subject><subject>nucleic acids</subject><subject>therapeutic targeting</subject><issn>1439-4227</issn><issn>1439-7633</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PwkAQhjdGI4hePWpP3oqzH922RywKJIgmgnjbLMuWrBSKu63Kv7dYot48zUzyvG8mD0LnGNoYgFyrmVFtAhAAUMwPUBMzGvshp_RwvzNCwgY6ce4VAGJO8TFqYM4iUkWaCN-XWWEK6ZZmvfBmW-_7fpeZXhdeYqwqM2m97qjjdTaFXGnrTtFRKjOnz_azhSZ3t-Ok7w8feoOkM_QVg4D7UtMgiCDlNOSA41kqQwWE67lmCnTA4lCygOh5yiXhVKrdZ1zOIxwzCimmtIWu6t6Nzd9K7QqxMk7pLJNrnZdO8DAkhEdBBbZrUNncOatTsbFmJe1WYBA7SWInSfxIqgIX--ZyttLzX3xvpQLiGvgwmd7-UyeSm0Hyt9yvs8YV-vMnK-2y-piGgZiOemIcR4_97stUPFf8Zc2nMhdyYY0TkycCmFbSGOGVjS_RB4nO</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Di Giusto, Daniel A</creator><creator>Knox, Sarah M</creator><creator>Lai, Yuching</creator><creator>Tyrelle, Gregory D</creator><creator>Aung, May T</creator><creator>King, Garry C</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</scope><scope>BSCLL</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>20060301</creationdate><title>Multitasking by Multivalent Circular DNA Aptamers</title><author>Di Giusto, Daniel A ; Knox, Sarah M ; Lai, Yuching ; Tyrelle, Gregory D ; Aung, May T ; King, Garry C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4056-ae35580f6376019bfa7c026ede4c0e5497a452edf6a263ac96316ad819430f133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aptamers, Nucleotide - chemistry</topic><topic>Cell Separation</topic><topic>Cells, Cultured</topic><topic>DNA structures</topic><topic>DNA, Circular - chemistry</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>immobilization</topic><topic>nanostructures</topic><topic>nucleic acids</topic><topic>therapeutic targeting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Giusto, Daniel A</creatorcontrib><creatorcontrib>Knox, Sarah M</creatorcontrib><creatorcontrib>Lai, Yuching</creatorcontrib><creatorcontrib>Tyrelle, Gregory D</creatorcontrib><creatorcontrib>Aung, May T</creatorcontrib><creatorcontrib>King, Garry C</creatorcontrib><collection>AGRIS</collection><collection>Istex</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>Chembiochem : a European journal of chemical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Giusto, Daniel A</au><au>Knox, Sarah M</au><au>Lai, Yuching</au><au>Tyrelle, Gregory D</au><au>Aung, May T</au><au>King, Garry C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multitasking by Multivalent Circular DNA Aptamers</atitle><jtitle>Chembiochem : a European journal of chemical biology</jtitle><addtitle>ChemBioChem</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>7</volume><issue>3</issue><spage>535</spage><epage>544</epage><pages>535-544</pages><issn>1439-4227</issn><eissn>1439-7633</eissn><abstract>Nucleic acid aptamers are finding increasing applications in biology, especially as therapeutic candidates and diagnostic components. An important characteristic in meeting the needs of these applications is improved stability in physiological fluids, which is most often accomplished with chemical modification or unnatural nucleotides. In an alternative approach we have specified the design of a multivalent circular DNA aptamer topology that encompasses a number of properties relevant to nucleic acid therapeutic candidates, especially the ability to multitask by combining different activities together within a modular structure. Improved stability in blood products, greater conformational stability, antidoting by complementary circular antiaptamers, heterovalency, transcription factor decoy activity and minimal unintended effects upon the cellular innate immune response are desirable properties that are described here. 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subjects | Aptamers, Nucleotide - chemistry Cell Separation Cells, Cultured DNA structures DNA, Circular - chemistry Flow Cytometry Humans immobilization nanostructures nucleic acids therapeutic targeting |
title | Multitasking by Multivalent Circular DNA Aptamers |
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