Hydrophilic labeling reagents of dipyrrylmethene-BF2 dyes for two-photon excited fluorometry:: Syntheses and photophysical characterization

被引:53
作者
Meltola, NJ
Wahlroos, R
Soini, AE
机构
[1] Univ Turku, Inst Biomed, Biophys Lab, Turku 20521, Finland
[2] Arctic Diagnost Oy, Turku 20521, Finland
关键词
two-photon excited fluorescence; dipyrrylmethene-BF2; BODIPY; synthesis; labeling; ArcDia TPX;
D O I
10.1023/B:JOFL.0000039350.94256.53
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recently introduced bioaffinity assay technology, ArcDia(TM)TPX, is based on two-photon excited fluorescence (TPE) and it enables separation-free ultra-sensitive immunoassays from microvolumes. Here we present syntheses of novel two-photon excitable fluorescent labeling reagents which have been specially designed to be used as label molecules in the ArcDia(TM)TPX assay technique. The labeling reagents are based on dipyrrylmetheneboron difluoride (dipyrrylmethene-BF2) chromophore, which have been substituted with aryl, heteroaryl or arylalkenyl chemical groups to extend the pi-electron conjugation. These substitutions results in a series of dipyrrylmethene-BF2 fluorophores with different photophysical properties. Dipyrrylmethene-BF2 fluorophores have been further substituted with a dipeptide linker unit and finally activated as succinimidyl esters to enable specific coupling with primary amino groups. The dipeptide linker serves as a spacer arm between the label and a target, and enhances the solubility of the label in aqueous solutions. Study of the chemical and photophysical performance of the new labeling reagents is described. The new labeling reagents exhibit high fluorescence quantum yields, and molar absorption coefficients. The results show that the new labels with the hydrophilic dipeptide linker unit provide large two-photon excitation cross-sections, high fluorescence quantum efficiency and good solubility in aqueous solutions. The results suggest that the novel dipyrrylmethene-BF2 labels are highly applicable to bioaffinity assays based on two-photon excitation of fluorescence.
引用
收藏
页码:635 / 647
页数:13
相关论文
共 29 条
[1]   FORMYLATION OF THE ARYLPYRROLE SERIES [J].
BOUKOUPOBA, JP ;
FARNIER, M ;
GUILARD, R .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1981, 59 (20) :2962-2967
[2]   A SYNTHESIS OF COPROPORPHYRIN .3. [J].
BULLOCK, E ;
JOHNSON, AW ;
MARKHAM, E ;
SHAW, KB .
JOURNAL OF THE CHEMICAL SOCIETY, 1958, (APR) :1430-1440
[3]   3,5-diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes:: Synthesis, spectroscopic, electrochemical, and structural properties [J].
Burghart, A ;
Kim, HJ ;
Welch, MB ;
Thoresen, LH ;
Reibenspies, J ;
Burgess, K ;
Bergstrom, F ;
Johansson, LBÅ .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (21) :7813-7819
[4]   Arylacetamide-derived fluorescent probes: Synthesis, biological evaluation, and direct fluorescent labeling of kappa opioid receptors in mouse microglial cells [J].
Chang, AC ;
Chao, CC ;
Takemori, AE ;
Gekker, G ;
Hu, SX ;
Peterson, PK ;
Portoghese, PS .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (08) :1729-1735
[5]   4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes modified for extended conjugation and restricted bond rotations [J].
Chen, J ;
Burghart, A ;
Derecskei-Kovacs, A ;
Burgess, K .
JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (10) :2900-2906
[6]   Two-photon-induced fluorescence from the phycoerythrin protein [J].
Chen, ZP ;
Kaplan, DL ;
Yang, K ;
Kumar, J ;
Marx, KA ;
Tripathy, SK .
APPLIED OPTICS, 1997, 36 (07) :1655-1659
[7]  
DEMAS JN, 1971, J PHYS CHEM-US, V75, P991, DOI 10.1021/j100678a001
[8]   A new microvolume technique for bioaffinity assays using two-photon excitation [J].
Hänninen, P ;
Soini, A ;
Meltola, N ;
Soini, J ;
Soukka, J ;
Soini, E .
NATURE BIOTECHNOLOGY, 2000, 18 (05) :548-550
[9]  
Haugland R.P., 1988, US pat, Patent No. [4,774,339, 4774339]
[10]  
Haugland R.P., 2002, Handbook of Fluorescent Probes and Research Products, V9th