Source:http://linkedlifedata.com/resource/pubmed/id/18198846
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2008-2-14
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pubmed:abstractText |
M13 virus particles were covalently attached to a planar gold-coated quartz crystal microbalance (QCM) through reaction with a self-assembled monolayer of N-hydroxysuccinimide thioctic ester, followed by incorporation of the blocking agent bovine serum albumin. This immobilization chemistry produced a phage multilayer having a coverage equivalent to approximately 6.5 close-packed monolayers of the virus. The properties of this "covalent virus surface" or CVS for the mass-based detection of a 148.2 kDa antibody were then evaluated in a phosphate buffer using a flow injection analysis system. The mass of the CVS increased with exposure to an antibody (p-Ab) known to bind the phage particles with high affinity. Bound p-Ab was removed by washing with 0.5 M HCl thereby regenerating the sensor surface. A calibration plot for p-Ab binding was constructed by repetitively exposing the surface to p-Ab at concentrations between 6.6 and 200 nM and HCl rinsing after each exposure. The mass-concentration relationship was linear with a sensitivity of 0.018 microg/(cm2 nM) and a limit of detection of 7 nM or 1.3 pmol. The CVS could be saturated with high doses of p-Ab enabling the determination that an average of approximately 140 binding sites are available per M13 phage particle. Exposure of the CVS to a second, nonbinding antibody (n-Ab) did not cause a measurable mass change. These results demonstrate that the covalent virus layer is a rugged, selective, and sensitive means for carrying out mass-based biodetection.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Buffers,
http://linkedlifedata.com/resource/pubmed/chemical/Esters,
http://linkedlifedata.com/resource/pubmed/chemical/Gold,
http://linkedlifedata.com/resource/pubmed/chemical/N-hydroxysuccinimide,
http://linkedlifedata.com/resource/pubmed/chemical/Quartz,
http://linkedlifedata.com/resource/pubmed/chemical/Serum Albumin, Bovine,
http://linkedlifedata.com/resource/pubmed/chemical/Succinimides
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0003-2700
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
80
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
933-43
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pubmed:meshHeading |
pubmed-meshheading:18198846-Antigen-Antibody Reactions,
pubmed-meshheading:18198846-Bacteriophage M13,
pubmed-meshheading:18198846-Biosensing Techniques,
pubmed-meshheading:18198846-Buffers,
pubmed-meshheading:18198846-Calibration,
pubmed-meshheading:18198846-Crystallization,
pubmed-meshheading:18198846-Esters,
pubmed-meshheading:18198846-Flow Injection Analysis,
pubmed-meshheading:18198846-Gold,
pubmed-meshheading:18198846-Molecular Weight,
pubmed-meshheading:18198846-Quartz,
pubmed-meshheading:18198846-Serum Albumin, Bovine,
pubmed-meshheading:18198846-Succinimides,
pubmed-meshheading:18198846-Surface Properties,
pubmed-meshheading:18198846-Time Factors
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pubmed:year |
2008
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pubmed:articleTitle |
Covalent virus layer for mass-based biosensing.
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pubmed:affiliation |
Department of Chemistry, University of California, Irvine, CA 92697-2025, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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