Loading…

Hydrogel glycan microarrays

The technology of hydrogel microchips manufacturing, which was developed previously for covalent immobilization of DNA and proteins, was applied for the preparation of glycochips and combined glyco/protein chips. Microchips consist of hydrogel drops separated with hydrophobic surface. Spacered amino...

Full description

Saved in:
Bibliographic Details
Published in:Analytical biochemistry 2005-12, Vol.347 (1), p.94-105
Main Authors: Dyukova, V.I., Dementieva, E.I., Zubtsov, D.A., Galanina, O.E., Bovin, N.V., Rubina, A.Yu
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23
cites cdi_FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23
container_end_page 105
container_issue 1
container_start_page 94
container_title Analytical biochemistry
container_volume 347
creator Dyukova, V.I.
Dementieva, E.I.
Zubtsov, D.A.
Galanina, O.E.
Bovin, N.V.
Rubina, A.Yu
description The technology of hydrogel microchips manufacturing, which was developed previously for covalent immobilization of DNA and proteins, was applied for the preparation of glycochips and combined glyco/protein chips. Microchips consist of hydrogel drops separated with hydrophobic surface. Spacered amino-saccharides and polyacrylamide glycoconjugates were used for immobilization. Gel elements were ∼1 nl in volume (150 μm in diameter and 25 μm in height), and the amount of covalently immobilized saccharide in the glycoarray was 0.4–1.7 pmol per gel element. Hydrogel glycan microchips were used for quantitative assay of antibodies against blood group antigens and assay of lectins with fluorescent detection. In all cases, only specific interaction with chip-immobilized saccharides was observed, whereas the background signal was very low. The detection limit of on-chip assays was comparable to that of the standard 96-well plate assays. Mixing of reaction solution allowed us to decrease the duration of the assays significantly: 2–3 h for incubation and development steps and 10 min for washing. A method for determination of association constants for binding of compounds with chip-immobilized ligands from the kinetics of their binding is proposed. Combined microchips containing different types of biomolecules can be designed and used for simultaneous detection of different compounds.
doi_str_mv 10.1016/j.ab.2005.09.009
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_20295314</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S000326970500672X</els_id><sourcerecordid>20295314</sourcerecordid><originalsourceid>FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23</originalsourceid><addsrcrecordid>eNp1kEFLAzEQhYMotlbvgiA9edt1kmyyjTcpaoWCFz2HbDIpKbvdmrTC_ntTWvAkDAwD7z3mfYTcUigpUPm4Lk1TMgBRgioB1BkZU1CyAA7qnIwBgBdMqnpErlJaA1BaCXlJRlQynmc2JneLwcV-he101Q7WbKZdsLE3MZohXZMLb9qEN6c9IV-vL5_zRbH8eHufPy8Ly2u1K1BwrBRaQ4Xn3Ljai9pTQ61xXlSN8zMFovKu4pVROPNKNszRfEnlUTjGJ-ThmLuN_fce0053IVlsW7PBfp80A6YEz44JgaMwv5hSRK-3MXQmDpqCPgDRa20afQCiQekMJFvuT9n7pkP3ZzgRyIKnowBzw5-AUScbcGPRhYh2p10f_k__BWS1btQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20295314</pqid></control><display><type>article</type><title>Hydrogel glycan microarrays</title><source>ScienceDirect Journals</source><creator>Dyukova, V.I. ; Dementieva, E.I. ; Zubtsov, D.A. ; Galanina, O.E. ; Bovin, N.V. ; Rubina, A.Yu</creator><creatorcontrib>Dyukova, V.I. ; Dementieva, E.I. ; Zubtsov, D.A. ; Galanina, O.E. ; Bovin, N.V. ; Rubina, A.Yu</creatorcontrib><description>The technology of hydrogel microchips manufacturing, which was developed previously for covalent immobilization of DNA and proteins, was applied for the preparation of glycochips and combined glyco/protein chips. Microchips consist of hydrogel drops separated with hydrophobic surface. Spacered amino-saccharides and polyacrylamide glycoconjugates were used for immobilization. Gel elements were ∼1 nl in volume (150 μm in diameter and 25 μm in height), and the amount of covalently immobilized saccharide in the glycoarray was 0.4–1.7 pmol per gel element. Hydrogel glycan microchips were used for quantitative assay of antibodies against blood group antigens and assay of lectins with fluorescent detection. In all cases, only specific interaction with chip-immobilized saccharides was observed, whereas the background signal was very low. The detection limit of on-chip assays was comparable to that of the standard 96-well plate assays. Mixing of reaction solution allowed us to decrease the duration of the assays significantly: 2–3 h for incubation and development steps and 10 min for washing. A method for determination of association constants for binding of compounds with chip-immobilized ligands from the kinetics of their binding is proposed. Combined microchips containing different types of biomolecules can be designed and used for simultaneous detection of different compounds.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2005.09.009</identifier><identifier>PMID: 16236238</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>ABO Blood-Group System - analysis ; Antibodies ; Antibodies, Monoclonal - chemistry ; Antibodies, Monoclonal - immunology ; Carbohydrates ; Combined glyco/protein chip ; Gel microchips ; Glycan microarrays ; Humans ; Hydrogel glycochips ; Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry ; Lectins ; Molecular Probes - chemistry ; Polysaccharides - chemistry ; Protein Array Analysis ; Ricin ; Ricin - chemistry ; Trisaccharides - chemistry</subject><ispartof>Analytical biochemistry, 2005-12, Vol.347 (1), p.94-105</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23</citedby><cites>FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16236238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dyukova, V.I.</creatorcontrib><creatorcontrib>Dementieva, E.I.</creatorcontrib><creatorcontrib>Zubtsov, D.A.</creatorcontrib><creatorcontrib>Galanina, O.E.</creatorcontrib><creatorcontrib>Bovin, N.V.</creatorcontrib><creatorcontrib>Rubina, A.Yu</creatorcontrib><title>Hydrogel glycan microarrays</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>The technology of hydrogel microchips manufacturing, which was developed previously for covalent immobilization of DNA and proteins, was applied for the preparation of glycochips and combined glyco/protein chips. Microchips consist of hydrogel drops separated with hydrophobic surface. Spacered amino-saccharides and polyacrylamide glycoconjugates were used for immobilization. Gel elements were ∼1 nl in volume (150 μm in diameter and 25 μm in height), and the amount of covalently immobilized saccharide in the glycoarray was 0.4–1.7 pmol per gel element. Hydrogel glycan microchips were used for quantitative assay of antibodies against blood group antigens and assay of lectins with fluorescent detection. In all cases, only specific interaction with chip-immobilized saccharides was observed, whereas the background signal was very low. The detection limit of on-chip assays was comparable to that of the standard 96-well plate assays. Mixing of reaction solution allowed us to decrease the duration of the assays significantly: 2–3 h for incubation and development steps and 10 min for washing. A method for determination of association constants for binding of compounds with chip-immobilized ligands from the kinetics of their binding is proposed. Combined microchips containing different types of biomolecules can be designed and used for simultaneous detection of different compounds.</description><subject>ABO Blood-Group System - analysis</subject><subject>Antibodies</subject><subject>Antibodies, Monoclonal - chemistry</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Carbohydrates</subject><subject>Combined glyco/protein chip</subject><subject>Gel microchips</subject><subject>Glycan microarrays</subject><subject>Humans</subject><subject>Hydrogel glycochips</subject><subject>Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry</subject><subject>Lectins</subject><subject>Molecular Probes - chemistry</subject><subject>Polysaccharides - chemistry</subject><subject>Protein Array Analysis</subject><subject>Ricin</subject><subject>Ricin - chemistry</subject><subject>Trisaccharides - chemistry</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp1kEFLAzEQhYMotlbvgiA9edt1kmyyjTcpaoWCFz2HbDIpKbvdmrTC_ntTWvAkDAwD7z3mfYTcUigpUPm4Lk1TMgBRgioB1BkZU1CyAA7qnIwBgBdMqnpErlJaA1BaCXlJRlQynmc2JneLwcV-he101Q7WbKZdsLE3MZohXZMLb9qEN6c9IV-vL5_zRbH8eHufPy8Ly2u1K1BwrBRaQ4Xn3Ljai9pTQ61xXlSN8zMFovKu4pVROPNKNszRfEnlUTjGJ-ThmLuN_fce0053IVlsW7PBfp80A6YEz44JgaMwv5hSRK-3MXQmDpqCPgDRa20afQCiQekMJFvuT9n7pkP3ZzgRyIKnowBzw5-AUScbcGPRhYh2p10f_k__BWS1btQ</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>Dyukova, V.I.</creator><creator>Dementieva, E.I.</creator><creator>Zubtsov, D.A.</creator><creator>Galanina, O.E.</creator><creator>Bovin, N.V.</creator><creator>Rubina, A.Yu</creator><general>Elsevier Inc</general><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></search><sort><creationdate>20051201</creationdate><title>Hydrogel glycan microarrays</title><author>Dyukova, V.I. ; Dementieva, E.I. ; Zubtsov, D.A. ; Galanina, O.E. ; Bovin, N.V. ; Rubina, A.Yu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>ABO Blood-Group System - analysis</topic><topic>Antibodies</topic><topic>Antibodies, Monoclonal - chemistry</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Carbohydrates</topic><topic>Combined glyco/protein chip</topic><topic>Gel microchips</topic><topic>Glycan microarrays</topic><topic>Humans</topic><topic>Hydrogel glycochips</topic><topic>Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry</topic><topic>Lectins</topic><topic>Molecular Probes - chemistry</topic><topic>Polysaccharides - chemistry</topic><topic>Protein Array Analysis</topic><topic>Ricin</topic><topic>Ricin - chemistry</topic><topic>Trisaccharides - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dyukova, V.I.</creatorcontrib><creatorcontrib>Dementieva, E.I.</creatorcontrib><creatorcontrib>Zubtsov, D.A.</creatorcontrib><creatorcontrib>Galanina, O.E.</creatorcontrib><creatorcontrib>Bovin, N.V.</creatorcontrib><creatorcontrib>Rubina, A.Yu</creatorcontrib><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><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dyukova, V.I.</au><au>Dementieva, E.I.</au><au>Zubtsov, D.A.</au><au>Galanina, O.E.</au><au>Bovin, N.V.</au><au>Rubina, A.Yu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrogel glycan microarrays</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>347</volume><issue>1</issue><spage>94</spage><epage>105</epage><pages>94-105</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>The technology of hydrogel microchips manufacturing, which was developed previously for covalent immobilization of DNA and proteins, was applied for the preparation of glycochips and combined glyco/protein chips. Microchips consist of hydrogel drops separated with hydrophobic surface. Spacered amino-saccharides and polyacrylamide glycoconjugates were used for immobilization. Gel elements were ∼1 nl in volume (150 μm in diameter and 25 μm in height), and the amount of covalently immobilized saccharide in the glycoarray was 0.4–1.7 pmol per gel element. Hydrogel glycan microchips were used for quantitative assay of antibodies against blood group antigens and assay of lectins with fluorescent detection. In all cases, only specific interaction with chip-immobilized saccharides was observed, whereas the background signal was very low. The detection limit of on-chip assays was comparable to that of the standard 96-well plate assays. Mixing of reaction solution allowed us to decrease the duration of the assays significantly: 2–3 h for incubation and development steps and 10 min for washing. A method for determination of association constants for binding of compounds with chip-immobilized ligands from the kinetics of their binding is proposed. Combined microchips containing different types of biomolecules can be designed and used for simultaneous detection of different compounds.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16236238</pmid><doi>10.1016/j.ab.2005.09.009</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0003-2697
ispartof Analytical biochemistry, 2005-12, Vol.347 (1), p.94-105
issn 0003-2697
1096-0309
language eng
recordid cdi_proquest_miscellaneous_20295314
source ScienceDirect Journals
subjects ABO Blood-Group System - analysis
Antibodies
Antibodies, Monoclonal - chemistry
Antibodies, Monoclonal - immunology
Carbohydrates
Combined glyco/protein chip
Gel microchips
Glycan microarrays
Humans
Hydrogel glycochips
Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry
Lectins
Molecular Probes - chemistry
Polysaccharides - chemistry
Protein Array Analysis
Ricin
Ricin - chemistry
Trisaccharides - chemistry
title Hydrogel glycan microarrays
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T17%3A05%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hydrogel%20glycan%20microarrays&rft.jtitle=Analytical%20biochemistry&rft.au=Dyukova,%20V.I.&rft.date=2005-12-01&rft.volume=347&rft.issue=1&rft.spage=94&rft.epage=105&rft.pages=94-105&rft.issn=0003-2697&rft.eissn=1096-0309&rft_id=info:doi/10.1016/j.ab.2005.09.009&rft_dat=%3Cproquest_cross%3E20295314%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c379t-e53e49eca15f33ad7f57f1a1cadf54bdf89054fd434a9e8f96b2d143469fe5d23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20295314&rft_id=info:pmid/16236238&rfr_iscdi=true