Detection of cell and tissue surface antigens using up-converting phosphors: A new reporter technology

被引:272
作者
Zijlmans, HJMAA [1 ]
Bonnet, J
Burton, J
Kardos, K
Vail, T
Niedbala, RS
Tanke, HJ
机构
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, Lab Cytochem & Cytometry, Leiden, Netherlands
[2] STC Technol Inc, Bethlehem, PA USA
关键词
luminescence; bioassays; diagnostic pathology; up-conversion; phosphors; autofluorescence; infrared light;
D O I
10.1006/abio.1998.2965
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel luminescent reporter for the sensitive detection of antigens in tissue sections or on cell membranes is described. It consists of submicron-size phosphor crystals (0.2-0.4 mu m), which are surface labeled with avidin or antibodies and capable of binding specifically to antigens on intact cells or in tissue sections. These phosphor reporters exhibit two-photon, anti-Stokes luminescence by up-converting infrared to visible light and are named Up-converting Phosphor Technology (UPT). They typically consist of yttriumoxysulfides doped with two different lanthanides exhibiting photostable, strong emission in the visible (blue, green, and red) upon excitation in the infrared. This report describes the conjugation of phosphor particles to NeutrAvidin with the subsequent use of this conjugate in a model system consisting of prostate-specific antigen in tissue sections and the CD4 membrane antigen on human lymphocytes. An epi-illumination fluorescence microscope was adapted to provide near-IR excitation using a xenon lamp for visualization of the visible emission. Advantages of UPT are (i) permanent, strong, anti-Stokes emission of discrete wavelengths; (ii) unmatched contrast in biological specimens due to the absence of autofluorescence upon excitation with IR light; (iii) simultaneous detection of multiple target analytes; and (iv) low-cost microscope modifications. The new methodology has not only high potential value in diagnostic pathology as described here, but may offer advantages for the detection of proteins or nucleic acids when applied to molecular biology, genomic research, virology, and microbiology. (C) 1999 Academic Press.
引用
收藏
页码:30 / 36
页数:7
相关论文
共 10 条
[1]   AUTOFLUORESCENCE OF VIABLE CULTURED MAMMALIAN-CELLS [J].
AUBIN, JE .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1979, 27 (01) :36-43
[2]   IMMUNOCHEMICAL DETECTION OF PROTEINS AND NUCLEIC-ACIDS ON FILTERS USING SMALL LUMINESCENT INORGANIC CRYSTALS AS MARKERS [J].
BEVERLOO, HB ;
VANSCHADEWIJK, A ;
ZIJLMANS, HJMAA ;
TANKE, HJ .
ANALYTICAL BIOCHEMISTRY, 1992, 203 (02) :326-334
[3]   A COMPARISON OF THE DETECTION SENSITIVITY OF LYMPHOCYTE MEMBRANE-ANTIGENS USING FLUORESCEIN AND PHOSPHOR IMMUNOCONJUGATES [J].
BEVERLOO, HB ;
VANSCHADEWIJK, A ;
ZIJLMANS, HJ ;
VERWOERD, NP ;
BONNETT, J ;
VROLIJK, H ;
TANKE, HJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (05) :719-725
[4]   INORGANIC PHOSPHORS AS NEW LUMINESCENT LABELS FOR IMMUNOCYTOCHEMISTRY AND TIME-RESOLVED MICROSCOPY [J].
BEVERLOO, HB ;
VANSCHADEWIJK, A ;
VANGELDERENBOELE, S ;
TANKE, HJ .
CYTOMETRY, 1990, 11 (07) :784-792
[5]  
HEMMILA I, 1982, FRESEN Z ANAL CHEM, V311, P352
[6]   LUMINESCENCE DIGITAL IMAGING MICROSCOPY [J].
JOVIN, TM ;
ARNDTJOVIN, DJ .
ANNUAL REVIEW OF BIOPHYSICS AND BIOPHYSICAL CHEMISTRY, 1989, 18 :271-308
[7]  
KRICKA LJ, 1994, CLIN CHEM, V40, P347
[8]  
TANKE HJ, 1986, Patent No. 8502187
[9]   USE OF FERROELECTRIC LIQUID-CRYSTAL SHUTTERS FOR TIME-RESOLVED FLUORESCENCE MICROSCOPY [J].
VERWOERD, NP ;
HENNINK, EJ ;
BONNET, J ;
VANDERGEEST, CRG ;
TANKE, HJ .
CYTOMETRY, 1994, 16 (02) :113-117
[10]  
Zarling D. A., 1997, United States Patent, Patent No. [5,674,698, 5674698]