Emission under hypoxia: One-electron reduction and fluorescence characteristics of an indolequinone-coumarin conjugate

被引:60
作者
Tanabe, Kazuhito [1 ]
Hirata, Nao [1 ]
Harada, Hiroshi [2 ,3 ]
Hiraoka, Masahiro [2 ,3 ]
Nishimoto, Sei-ichi [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Radiat Oncol & Image Appl Therapy, Sakyo Ku, Kyoto 6068507, Japan
[3] Kyoto Univ, Nanomed Merger Educ Unit, Sakyo Ku, Kyoto 6068507, Japan
关键词
enzymes; fluorescent probes; hypoxia; indolequinones; one-electron reduction;
D O I
10.1002/cbic.200700458
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A characteristic feature of the reactivity of indolequinone derivatives, substituents of which can be removed by one-electron reduction under hypoxic conditions, was applied to the development of a new class of fluorescent probes for disease-relevant hypoxia. A reducing indolequinone parent molecule conjugated with fluorescent coumarin chromophores could suppress efficiently the fluorescence emission of the coumarin moieties by an intramolecular electron-transfer quenching mechanism and a conventional internal-filter effect. Under hypoxic conditions, however, the conjugate, denoted IQ-Cou, underwent a one-electron reduction triggered by X irradiation or the action of a reduction enzyme to release a fluorescent coumarin chromophore, whereupon an intense fluorescence emission with a maximum intensity at 420 nm was observed. The one-electron reduction of IQ-Cou was suppressed by molecular oxygen under aerobic conditions. IQ-Cou also showed intense fluorescence in a hypoxia-selective manner upon incubation with a cell lysate of the human fibrosarcoma cell line HT-1080. The IQ-Cou conjugate has several unique properties that are favorable for a fluorescent probe of hypoxia-specific imaging.
引用
收藏
页码:426 / 432
页数:7
相关论文
共 30 条
[1]   Electron-transfer reactions in micelles: Dynamics of psoralen and coumarin radical cations [J].
Chen, L ;
Wood, PD ;
Mnyusiwalla, A ;
Marlinga, J ;
Johnston, LJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (44) :10927-10935
[2]   Hypoxia targeted gene therapy to increase the efficacy of tirapazamine as an adjuvant to radiotherapy: Reversing tumor radioresistance and effecting cure [J].
Cowen, RL ;
Williams, KJ ;
Chinje, EC ;
Jaffar, M ;
Sheppard, FCD ;
Telfer, BA ;
Wind, NS ;
Stratford, IJ .
CANCER RESEARCH, 2004, 64 (04) :1396-1402
[3]   Modifying rates of reductive elimination of leaving groups from indolequinone prodrugs: a key factor in controlling hypoxia-selective drug release [J].
Everett, SA ;
Swann, E ;
Naylor, MA ;
Stratford, MRL ;
Patel, KB ;
Tian, N ;
Newman, RG ;
Vojnovic, B ;
Moody, CJ ;
Wardman, P .
BIOCHEMICAL PHARMACOLOGY, 2002, 63 (09) :1629-1639
[4]   REACTION-MECHANISMS IN THE RADIOLYSIS OF PEPTIDES, POLYPEPTIDES, AND PROTEINS [J].
GARRISON, WM .
CHEMICAL REVIEWS, 1987, 87 (02) :381-398
[5]   Hypoxia - A key regulatory factor in tumour growth [J].
Harris, AL .
NATURE REVIEWS CANCER, 2002, 2 (01) :38-47
[6]   REACTIONS OF CARBONYLIC COMPOUNDS WITH HYDRATED ELECTRONS [J].
HART, EJ ;
FIELDEN, EM ;
ANBAR, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1967, 71 (12) :3993-&
[7]   Design, synthesis, and biological evaluation of indolequinone phosphoramidate prodrugs targeted to DT-diaphorase [J].
Hernick, M ;
Flader, C ;
Borch, RF .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (16) :3540-3548
[8]  
Kavarnos G.J., 1993, Fundamentals of Photoinduced Electron Transfer
[9]   Tumor hypoxia: A target for selective cancer therapy [J].
Kizaka-Kondoh, S ;
Inoue, M ;
Harada, H ;
Hiraoka, M .
CANCER SCIENCE, 2003, 94 (12) :1021-1028
[10]   Rational design principle for modulating fluorescence properties of fluorescein-based probes by photoinduced electron transfer [J].
Miura, T ;
Urano, Y ;
Tanaka, K ;
Nagano, T ;
Ohkubo, K ;
Fukuzumi, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (28) :8666-8671