Phosphorescent platinum/palladium coproporphyrins for time-resolved luminescence microscopy

被引:45
作者
de Haas, RR
van Gijlswijk, RPM
van der Tol, EB
Veuskens, J
van Gijssel, HE
Tijdens, RB
Bonnet, J
Verwoerd, NP
Tanke, HJ
机构
[1] Leiden Univ, Med Ctr, Sylvius Labs, Dept Mol Cell Biol,Lab Cytochem & Cytometry, NL-2333 AL Leiden, Netherlands
[2] Univ Amsterdam, Dept Organ Chem, Amsterdam, Netherlands
[3] Univ Amsterdam, Inst Mol Cell Biol, NL-1012 WX Amsterdam, Netherlands
[4] Leiden Univ, Sylvius Labs, Leiden Amsterdam Ctr Drug Res, Div Toxicol, Leiden, Netherlands
关键词
metalloporphyrins; time-resolved luminescence microscopy; phosphorescence; autofluorescence; FISH; bleaching; tyramide signal amplification;
D O I
10.1177/002215549904700207
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Streptavidin and antibodies were labeled with phosphorescent platinum and palladium coproporphyrin. The optimal conjugates were selected on the basis of spectroscopic analysis (molar extinction coefficient, quantum yield, lifetime) and using ELISA assays to determine the retention of biological activity and immunospecificity. They were subsequently tested for the detection of prostate-specific antigen, glucagon, human androgen receptor, p53, and glutathione transferase in strongly autofluorescent tissues. Furthermore, platinum and palladium coproporphyrin-labeled dUTPs were synthesized for the enzymatic labeling of DNA probes. Porphyrin-labeled DNA probes and porphyrin-labeled streptavidin conjugates were evaluated for DNA in situ hybridization oh metaphase spreads, using direct and indirect methods, respectively. The developed in situ detection technology is shown to be applicable not only in mammals but also in plants. A modular-based time-resolved microscope was constructed and used for the evaluation of porphyrin-stained samples. The time-resolved module was found suitable for detection of antigens and DNA targets in an autofluorescent environment. Higher image contrasts were generally obtained in comparison with conventional detection systems (e.g., fourfold improvement in detection of glutathione transferase).
引用
收藏
页码:183 / 196
页数:14
相关论文
共 28 条
[1]   BIOTIN AMPLIFICATION OF BIOTIN AND HORSERADISH-PEROXIDASE SIGNALS IN HISTOCHEMICAL STAINS [J].
ADAMS, JC .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (10) :1457-1463
[2]   CATALYZED REPORTER DEPOSITION, A NOVEL METHOD OF SIGNAL AMPLIFICATION - APPLICATION TO IMMUNOASSAYS [J].
BOBROW, MN ;
HARRIS, TD ;
SHAUGHNESSY, KJ ;
LITT, GJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 125 (1-2) :279-285
[3]   NUCLEAR-LOCALIZATION OF THE PETUNIA MADS BOX PROTEIN FBP1 [J].
CANAS, LA ;
BUSSCHER, M ;
ANGENENT, GC ;
BELTRAN, JP ;
VANTUNEN, AJ .
PLANT JOURNAL, 1994, 6 (04) :597-604
[4]   CLONING OF HUMAN SATELLITE-III DNA - DIFFERENT COMPONENTS ARE ON DIFFERENT CHROMOSOMES [J].
COOKE, HJ ;
HINDLEY, J .
NUCLEIC ACIDS RESEARCH, 1979, 6 (10) :3177-3197
[5]   Platinum porphyrins as phosphorescent label for time-resolved microscopy [J].
deHaas, RR ;
vanGijlswijk, RPM ;
vanderTol, EB ;
Zijlmans, HJMAA ;
BakkerSchut, T ;
Bonnet, J ;
Verwoerd, NP ;
Tanke, HJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1997, 45 (09) :1279-1292
[6]   The use of peroxidase-mediated deposition of biotin-tyramide in combination with time-resolved fluorescence imaging of europium chelate label in immunohistochemistry and in situ hybridization [J].
deHaas, RR ;
Verwoerd, NP ;
vanderCorput, MP ;
vanGijlswijk, RP ;
Siitari, H ;
Tanke, HJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1996, 44 (10) :1091-1099
[7]  
DEWINTER JAR, 1990, J PATHOL, V161, P329
[8]   ANALYSIS OF ANTIFADING REAGENTS FOR FLUORESCENCE MICROSCOPY [J].
FLORIJN, RJ ;
SLATS, J ;
TANKE, HJ ;
RAAP, AK .
CYTOMETRY, 1995, 19 (02) :177-182
[9]  
JOVIN TM, 1989, ANN REV BIOPHYS CHEM, V18, P217
[10]   THE CHALCONE SYNTHASE MULTIGENE FAMILY OF PETUNIA-HYBRIDA (V30) - DIFFERENTIAL, LIGHT-REGULATED EXPRESSION DURING FLOWER DEVELOPMENT AND UV-LIGHT INDUCTION [J].
KOES, RE ;
SPELT, CE ;
MOL, JNM .
PLANT MOLECULAR BIOLOGY, 1989, 12 (02) :213-225