Site-specific protein immobilization in a microfluidic chip channel via an IEF-gelation process
A novel strategy for site‐specific protein immobilization via combining chip IEF with low‐temperature sol–gel technology, called IEF–GEL here, in the channel of a modified poly(methyl methacrylate) (PMMA) microfluidic chip is proposed in this work. The IEF–GEL process involves firstly IEF for homoge...
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description | A novel strategy for site‐specific protein immobilization via combining chip IEF with low‐temperature sol–gel technology, called IEF–GEL here, in the channel of a modified poly(methyl methacrylate) (PMMA) microfluidic chip is proposed in this work. The IEF–GEL process involves firstly IEF for homogeneously dissolved protein in PBS containing alumina sol and carrier ampholyte with prearranged pH gradient, and then gelation locally for protein encapsulation. The process and feasibility of proposed IEF–GEL were investigated by EOF measurements, fluorescence microscopic photography, Raman spectrum and further demonstrated by glucose oxidase (GOx) reactors integrated with end‐column electrochemical detection. Site‐controllable immobilization of protein was realized in a 30 mm long microfluidic chip channel by the strategy to create a ∼1.7 mm concentrated FITC‐BSA band, which leads to great improvement of the elute peak shape, accomplished with remarkably increased sensitivity, ∼20 times higher than that without IEF–GEL treatment to GOx reactors. The kinetic response of GOx after IEF–GEL treatment was also investigated. The proposed system holds the advantages of IEF and low‐temperature sol–gel technologies, i.e. concentrating the protein to be focused and retaining the biological activity for the gel‐embedded protein, thus realizes site‐specific immobilization of low‐concentration protein at nL volume level. |
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The IEF–GEL process involves firstly IEF for homogeneously dissolved protein in PBS containing alumina sol and carrier ampholyte with prearranged pH gradient, and then gelation locally for protein encapsulation. The process and feasibility of proposed IEF–GEL were investigated by EOF measurements, fluorescence microscopic photography, Raman spectrum and further demonstrated by glucose oxidase (GOx) reactors integrated with end‐column electrochemical detection. Site‐controllable immobilization of protein was realized in a 30 mm long microfluidic chip channel by the strategy to create a ∼1.7 mm concentrated FITC‐BSA band, which leads to great improvement of the elute peak shape, accomplished with remarkably increased sensitivity, ∼20 times higher than that without IEF–GEL treatment to GOx reactors. The kinetic response of GOx after IEF–GEL treatment was also investigated. The proposed system holds the advantages of IEF and low‐temperature sol–gel technologies, i.e. concentrating the protein to be focused and retaining the biological activity for the gel‐embedded protein, thus realizes site‐specific immobilization of low‐concentration protein at nL volume level.</description><identifier>ISSN: 0173-0835</identifier><identifier>EISSN: 1522-2683</identifier><identifier>DOI: 10.1002/elps.200600569</identifier><identifier>PMID: 17447236</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Ampholyte Mixtures - chemistry ; Electrophoresis, Microchip - instrumentation ; Electrophoresis, Microchip - methods ; Fluorescein-5-isothiocyanate - analogs & derivatives ; Fluorescein-5-isothiocyanate - chemistry ; Gels - chemical synthesis ; Gels - chemistry ; IEF ; Immobilized protein ; Indicators and Reagents ; Isoelectric Focusing - methods ; Kinetics ; Microfluidics - methods ; Polymethyl Methacrylate - chemical synthesis ; Polymethyl Methacrylate - chemistry ; Proteins - chemistry ; Sensitivity and Specificity ; Serum Albumin, Bovine - chemistry ; Site-specific ; Sol-gel ; Temperature</subject><ispartof>Electrophoresis, 2007-05, Vol.28 (10), p.1587-1594</ispartof><rights>Copyright © 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5099-4873c79e216aaba5ed13dcfa743cce5dd4075005929c32eb6e18b622ec1c6e3b3</citedby><cites>FETCH-LOGICAL-c5099-4873c79e216aaba5ed13dcfa743cce5dd4075005929c32eb6e18b622ec1c6e3b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Felps.200600569$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Felps.200600569$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17447236$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Mianhong</creatorcontrib><creatorcontrib>Peng, Youyuan</creatorcontrib><creatorcontrib>Yu, Shaoning</creatorcontrib><creatorcontrib>Liu, Baohong</creatorcontrib><creatorcontrib>Kong, Jilie</creatorcontrib><title>Site-specific protein immobilization in a microfluidic chip channel via an IEF-gelation process</title><title>Electrophoresis</title><addtitle>ELECTROPHORESIS</addtitle><description>A novel strategy for site‐specific protein immobilization via combining chip IEF with low‐temperature sol–gel technology, called IEF–GEL here, in the channel of a modified poly(methyl methacrylate) (PMMA) microfluidic chip is proposed in this work. The IEF–GEL process involves firstly IEF for homogeneously dissolved protein in PBS containing alumina sol and carrier ampholyte with prearranged pH gradient, and then gelation locally for protein encapsulation. The process and feasibility of proposed IEF–GEL were investigated by EOF measurements, fluorescence microscopic photography, Raman spectrum and further demonstrated by glucose oxidase (GOx) reactors integrated with end‐column electrochemical detection. Site‐controllable immobilization of protein was realized in a 30 mm long microfluidic chip channel by the strategy to create a ∼1.7 mm concentrated FITC‐BSA band, which leads to great improvement of the elute peak shape, accomplished with remarkably increased sensitivity, ∼20 times higher than that without IEF–GEL treatment to GOx reactors. The kinetic response of GOx after IEF–GEL treatment was also investigated. The proposed system holds the advantages of IEF and low‐temperature sol–gel technologies, i.e. concentrating the protein to be focused and retaining the biological activity for the gel‐embedded protein, thus realizes site‐specific immobilization of low‐concentration protein at nL volume level.</description><subject>Ampholyte Mixtures - chemistry</subject><subject>Electrophoresis, Microchip - instrumentation</subject><subject>Electrophoresis, Microchip - methods</subject><subject>Fluorescein-5-isothiocyanate - analogs & derivatives</subject><subject>Fluorescein-5-isothiocyanate - chemistry</subject><subject>Gels - chemical synthesis</subject><subject>Gels - chemistry</subject><subject>IEF</subject><subject>Immobilized protein</subject><subject>Indicators and Reagents</subject><subject>Isoelectric Focusing - methods</subject><subject>Kinetics</subject><subject>Microfluidics - methods</subject><subject>Polymethyl Methacrylate - chemical synthesis</subject><subject>Polymethyl Methacrylate - chemistry</subject><subject>Proteins - chemistry</subject><subject>Sensitivity and Specificity</subject><subject>Serum Albumin, Bovine - chemistry</subject><subject>Site-specific</subject><subject>Sol-gel</subject><subject>Temperature</subject><issn>0173-0835</issn><issn>1522-2683</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtP3DAURq2Kqkyh2y6rrNhlev1OlhUdKOqIUtEKdpbj3BRT50GcaYFfj1FGtLvZ2LJ0vmPd-xHynsKSArCPGIa4ZAAKQKryFVlQyVjOVMH3yAKo5jkUXO6TtzHeAoAohXhD9qkWQjOuFsRc-gnzOKDzjXfZMPYT-i7zbdtXPvhHO_k-PbvMZq13Y9-Eja8T6G78kA7bdRiyP95mtsvOVif5LwxzJJkcxnhIXjc2RHy3vQ_Iz5PVj-Mv-frb6dnxp3XuJJRlLgrNnS6RUWVtZSXWlNeusVpw51DWtQAt04glKx1nWCmkRaUYQ0edQl7xA3I0e9O_dxuMk2l9dBiC7bDfRKNBcsE07AR52qVmotgJMhDAgMsELmcwrSfGERszjL6144OhYJ5LMs8lmZeSUuDD1rypWqz_4dtWElDOwF8f8GGHzqzWF5f_y_M56-OE9y9ZO_42SnMtzdX5qfl-vv76WV9cG86fAHEcrg0</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Shi, Mianhong</creator><creator>Peng, Youyuan</creator><creator>Yu, Shaoning</creator><creator>Liu, Baohong</creator><creator>Kong, Jilie</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7QF</scope><scope>7U5</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20070501</creationdate><title>Site-specific protein immobilization in a microfluidic chip channel via an IEF-gelation process</title><author>Shi, Mianhong ; Peng, Youyuan ; Yu, Shaoning ; Liu, Baohong ; Kong, Jilie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5099-4873c79e216aaba5ed13dcfa743cce5dd4075005929c32eb6e18b622ec1c6e3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Ampholyte Mixtures - chemistry</topic><topic>Electrophoresis, Microchip - instrumentation</topic><topic>Electrophoresis, Microchip - methods</topic><topic>Fluorescein-5-isothiocyanate - analogs & derivatives</topic><topic>Fluorescein-5-isothiocyanate - chemistry</topic><topic>Gels - chemical synthesis</topic><topic>Gels - chemistry</topic><topic>IEF</topic><topic>Immobilized protein</topic><topic>Indicators and Reagents</topic><topic>Isoelectric Focusing - methods</topic><topic>Kinetics</topic><topic>Microfluidics - methods</topic><topic>Polymethyl Methacrylate - chemical synthesis</topic><topic>Polymethyl Methacrylate - chemistry</topic><topic>Proteins - chemistry</topic><topic>Sensitivity and Specificity</topic><topic>Serum Albumin, Bovine - chemistry</topic><topic>Site-specific</topic><topic>Sol-gel</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Mianhong</creatorcontrib><creatorcontrib>Peng, Youyuan</creatorcontrib><creatorcontrib>Yu, Shaoning</creatorcontrib><creatorcontrib>Liu, Baohong</creatorcontrib><creatorcontrib>Kong, Jilie</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Aluminium Industry Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Electrophoresis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Mianhong</au><au>Peng, Youyuan</au><au>Yu, Shaoning</au><au>Liu, Baohong</au><au>Kong, Jilie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Site-specific protein immobilization in a microfluidic chip channel via an IEF-gelation process</atitle><jtitle>Electrophoresis</jtitle><addtitle>ELECTROPHORESIS</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>28</volume><issue>10</issue><spage>1587</spage><epage>1594</epage><pages>1587-1594</pages><issn>0173-0835</issn><eissn>1522-2683</eissn><abstract>A novel strategy for site‐specific protein immobilization via combining chip IEF with low‐temperature sol–gel technology, called IEF–GEL here, in the channel of a modified poly(methyl methacrylate) (PMMA) microfluidic chip is proposed in this work. The IEF–GEL process involves firstly IEF for homogeneously dissolved protein in PBS containing alumina sol and carrier ampholyte with prearranged pH gradient, and then gelation locally for protein encapsulation. The process and feasibility of proposed IEF–GEL were investigated by EOF measurements, fluorescence microscopic photography, Raman spectrum and further demonstrated by glucose oxidase (GOx) reactors integrated with end‐column electrochemical detection. Site‐controllable immobilization of protein was realized in a 30 mm long microfluidic chip channel by the strategy to create a ∼1.7 mm concentrated FITC‐BSA band, which leads to great improvement of the elute peak shape, accomplished with remarkably increased sensitivity, ∼20 times higher than that without IEF–GEL treatment to GOx reactors. The kinetic response of GOx after IEF–GEL treatment was also investigated. The proposed system holds the advantages of IEF and low‐temperature sol–gel technologies, i.e. concentrating the protein to be focused and retaining the biological activity for the gel‐embedded protein, thus realizes site‐specific immobilization of low‐concentration protein at nL volume level.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>17447236</pmid><doi>10.1002/elps.200600569</doi><tpages>8</tpages></addata></record> |
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subjects | Ampholyte Mixtures - chemistry Electrophoresis, Microchip - instrumentation Electrophoresis, Microchip - methods Fluorescein-5-isothiocyanate - analogs & derivatives Fluorescein-5-isothiocyanate - chemistry Gels - chemical synthesis Gels - chemistry IEF Immobilized protein Indicators and Reagents Isoelectric Focusing - methods Kinetics Microfluidics - methods Polymethyl Methacrylate - chemical synthesis Polymethyl Methacrylate - chemistry Proteins - chemistry Sensitivity and Specificity Serum Albumin, Bovine - chemistry Site-specific Sol-gel Temperature |
title | Site-specific protein immobilization in a microfluidic chip channel via an IEF-gelation process |
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