rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
6
|
pubmed:dateCreated |
2004-7-26
|
pubmed:abstractText |
Fluorescein-labeled antibodies are widely used in clinical assays and fluorescence microscopy. The fluorescent signal per labeled antibody is limited by fluorescein self-quenching, which occurs when the antibody is heavily labeled with multiple fluoresceins. We examined immunoglobulin G (IgG) when labeled with 0.7 to about 30 fluoresceins per antibody molecule. The extent of self-quenching was decreased, and the signal increased, when the labeled antibody was in close proximity to metallic silver particles. Time-resolved measurements showed that the intensity increase was due in part to a silver-induced increase in the radiative decay rate. These results suggest the use of labeled antibodies conjugated to silver particles as ultrabright probes for imaging or analytical applications.
|
pubmed:grant |
|
pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0006-3525
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
74
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
467-75
|
pubmed:dateRevised |
2011-5-17
|
pubmed:meshHeading |
pubmed-meshheading:15274090-Antibodies,
pubmed-meshheading:15274090-Fluorescein,
pubmed-meshheading:15274090-Fluorescein-5-isothiocyanate,
pubmed-meshheading:15274090-Fluorescent Dyes,
pubmed-meshheading:15274090-Humans,
pubmed-meshheading:15274090-Image Processing, Computer-Assisted,
pubmed-meshheading:15274090-Immunoglobulin G,
pubmed-meshheading:15274090-Indicators and Reagents,
pubmed-meshheading:15274090-Microscopy, Fluorescence,
pubmed-meshheading:15274090-Models, Statistical,
pubmed-meshheading:15274090-Silver,
pubmed-meshheading:15274090-Spectrophotometry,
pubmed-meshheading:15274090-Time Factors
|
pubmed:year |
2004
|
pubmed:articleTitle |
Ultrabright fluorescein-labeled antibodies near silver metallic surfaces.
|
pubmed:affiliation |
Center for Fluorescence Spectroscopy, University of Maryland at Baltimore, Department of Biochemistry, 725 West Lombard Street, Baltimore, MD 21201, USA. lakowicz@cfs.umbi.umd.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|