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Luminol encapsulated liposome as a signal generator for the detection of specific antigen-antibody reactions and nucleotide hybridization.

Identifieur interne : 000764 ( Ncbi/Curation ); précédent : 000763; suivant : 000765

Luminol encapsulated liposome as a signal generator for the detection of specific antigen-antibody reactions and nucleotide hybridization.

Auteurs : Pakavadee Rakthong [Thaïlande] ; Akarin Intaramat ; Kavi Ratanabanangkoon

Source :

RBID : pubmed:20631437

Descripteurs français

English descriptors

Abstract

Liposomes prepared with biotinylated phospholipids and luminol entrapped were shown to be of 187 nm in size, 59% of which were unilamellar and with 43% luminol trapping efficiency. Liposome prepared from biotinylated phospholipids with a longer hydrophilic PEG2000 spacer, but not with the shorter hydrophobic caproyl one, bound efficiently and specifically with immobilized streptavidin in a microplate assay. The interactions of dinitrophenol and tobramycin with their respective antibodies, and the hybridization of 20-mers oligonucleotides were studied using the liposome as a signal generator. These reactions were shown to be specific with limits of detection of 0.58 microM, 0.96 microM and 18 nM, respectively.

DOI: 10.2116/analsci.26.767
PubMed: 20631437

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Le document en format XML

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<nlm:affiliation>Department of Microbiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.</nlm:affiliation>
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<name sortKey="Ratanabanangkoon, Kavi" sort="Ratanabanangkoon, Kavi" uniqKey="Ratanabanangkoon K" first="Kavi" last="Ratanabanangkoon">Kavi Ratanabanangkoon</name>
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<term>Antigen-Antibody Complex (analysis)</term>
<term>Antigen-Antibody Complex (immunology)</term>
<term>Antigen-Antibody Reactions (immunology)</term>
<term>Base Sequence</term>
<term>Biosensing Techniques (methods)</term>
<term>Biotinylation</term>
<term>Feasibility Studies</term>
<term>Immobilized Proteins (chemistry)</term>
<term>Light</term>
<term>Liposomes (chemistry)</term>
<term>Luminol (chemistry)</term>
<term>Nucleic Acid Hybridization</term>
<term>Oligonucleotides (chemistry)</term>
<term>Oligonucleotides (genetics)</term>
<term>Phosphatidylethanolamines (chemistry)</term>
<term>Polyethylene Glycols (chemistry)</term>
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<term>Biotinylation</term>
<term>Complexe antigène-anticorps (analyse)</term>
<term>Complexe antigène-anticorps (immunologie)</term>
<term>Diffusion de rayonnements</term>
<term>Hybridation d'acides nucléiques</term>
<term>Liposomes ()</term>
<term>Luminol ()</term>
<term>Lumière</term>
<term>Oligonucléotides ()</term>
<term>Oligonucléotides (génétique)</term>
<term>Phosphatidyléthanolamine ()</term>
<term>Polyéthylène glycols ()</term>
<term>Propriétés de surface</term>
<term>Protéines immobilisées ()</term>
<term>Réaction antigène-anticorps (immunologie)</term>
<term>Spécificité des anticorps (immunologie)</term>
<term>Streptavidine ()</term>
<term>Séquence nucléotidique</term>
<term>Techniques de biocapteur ()</term>
<term>Études de faisabilité</term>
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<term>Antigen-Antibody Complex</term>
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<term>Immobilized Proteins</term>
<term>Liposomes</term>
<term>Luminol</term>
<term>Oligonucleotides</term>
<term>Phosphatidylethanolamines</term>
<term>Polyethylene Glycols</term>
<term>Streptavidin</term>
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<term>Complexe antigène-anticorps</term>
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<term>Oligonucléotides</term>
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<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Complexe antigène-anticorps</term>
<term>Réaction antigène-anticorps</term>
<term>Spécificité des anticorps</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Antibody Specificity</term>
<term>Antigen-Antibody Complex</term>
<term>Antigen-Antibody Reactions</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Biosensing Techniques</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Base Sequence</term>
<term>Biotinylation</term>
<term>Feasibility Studies</term>
<term>Light</term>
<term>Nucleic Acid Hybridization</term>
<term>Scattering, Radiation</term>
<term>Surface Properties</term>
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<term>Biotinylation</term>
<term>Diffusion de rayonnements</term>
<term>Hybridation d'acides nucléiques</term>
<term>Liposomes</term>
<term>Luminol</term>
<term>Lumière</term>
<term>Oligonucléotides</term>
<term>Phosphatidyléthanolamine</term>
<term>Polyéthylène glycols</term>
<term>Propriétés de surface</term>
<term>Protéines immobilisées</term>
<term>Streptavidine</term>
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<term>Techniques de biocapteur</term>
<term>Études de faisabilité</term>
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<div type="abstract" xml:lang="en">Liposomes prepared with biotinylated phospholipids and luminol entrapped were shown to be of 187 nm in size, 59% of which were unilamellar and with 43% luminol trapping efficiency. Liposome prepared from biotinylated phospholipids with a longer hydrophilic PEG2000 spacer, but not with the shorter hydrophobic caproyl one, bound efficiently and specifically with immobilized streptavidin in a microplate assay. The interactions of dinitrophenol and tobramycin with their respective antibodies, and the hybridization of 20-mers oligonucleotides were studied using the liposome as a signal generator. These reactions were shown to be specific with limits of detection of 0.58 microM, 0.96 microM and 18 nM, respectively.</div>
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