8-Hydroxyquinoline derivatives as fluorescent sensors for magnesium in living cells

被引:276
作者
Farruggia, G
Iotti, S
Prodi, L
Montalti, M
Zaccheroni, N
Savage, PB
Trapani, V
Sale, P
Wolf, FI
机构
[1] Univ Bologna, Dipartimento Biochim G Moruzzi, I-40126 Bologna, Italy
[2] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
[3] Univ Bologna, Dipartimento Med Clin & Biotecnol Appl D Campanac, I-40138 Bologna, Italy
[4] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
[5] Univ Cattolica Sacro Cuore, Ist Patol Gen, I-00168 Rome, Italy
[6] Univ Cattolica Sacro Cuore, Ctr Ric Oncol Giovanni XXIII, I-00168 Rome, Italy
关键词
D O I
10.1021/ja056523u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the key role of magnesium in many fundamental biological processes, knowledge about its intracellular regulation is still scarce, due to the lack of appropriate detection methods. Here, we report the spectroscopic and photochemical characterization of two diaza-18-crown-6 hydroxyquinoline derivatives (DCHQ) and we propose their application in total Mg2+ assessment and in confocal imaging as effective Mg2+ indicators. DCHQ derivatives 1 and 2 bind Mg2+ with much higher affinity than other available probes (K-d = 44 and 73 mu M, respectively) and show a strong fluorescence increase upon binding. Remarkably, fluorescence output is not significantly affected by other divalent cations, most importantly Ca2+, or by pH changes within the physiological range. Evidence is provided on the use of fluorometric data to derive total cellular Mg2+ content, which is consistent with atomic absorption data. Furthermore, we show that DCHQ compounds can be effectively employed to map intracellular ion distribution and movements in live cells by confocal microscopy. A clear staining pattern consistent with known affinities of Mg2+ for biological ligands is shown; moreover, changes in the fluorescence signal could be tracked following stimuli known to modify intracellular Mg2+ concentration. These findings suggest that DCHQ derivatives may serve as new tools for the study of Mg2+ regulation, allowing sensitive and straightforward detection of both static and dynamic signals.
引用
收藏
页码:344 / 350
页数:7
相关论文
共 50 条
[1]  
[Anonymous], MAGNESIUM CELL
[2]   PROTOTROPIC EQUILIBRIUM + FLUORESCENCE OF SOME 8-HYDROXYQUINOLINE DERIVATIVES [J].
BALLARD, RE ;
EDWARDS, JW .
JOURNAL OF THE CHEMICAL SOCIETY, 1964, (DEC) :4868-&
[3]   PHOSPHORESCENT 8-QUINOLINOL METAL-CHELATES - EXCITED-STATE PROPERTIES AND REDOX BEHAVIOR [J].
BALLARDINI, R ;
VARANI, G ;
INDELLI, MT ;
SCANDOLA, F .
INORGANIC CHEMISTRY, 1986, 25 (22) :3858-3865
[4]   Excited-state processes in 8-hydroxyquinoline: Photoinduced tautomerization and solvation effects [J].
Bardez, E ;
Devol, I ;
Larrey, B ;
Valeur, B .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (39) :7786-7793
[5]  
Barker PB, 1999, MAGNET RESON MED, V41, P400, DOI 10.1002/(SICI)1522-2594(199902)41:2<400::AID-MRM26>3.0.CO
[6]  
2-E
[7]  
BOND M, 1987, J BIOL CHEM, V262, P15630
[8]   Synthesis and properties of 5-chloro-8-hydroxyquinoline-substituted azacrown ethers: A new family of highly metal ion-selective lariat ethers [J].
Bordunov, AV ;
Bradshaw, JS ;
Zhang, XX ;
Dalley, NK ;
Kou, XL ;
Izatt, RM .
INORGANIC CHEMISTRY, 1996, 35 (25) :7229-7240
[9]   Origins of 'on-off' fluorescent behavior of 8-hydroxyquinoline containing chemosensors [J].
Bronson, RT ;
Montalti, M ;
Prodi, L ;
Zaccheroni, N ;
Lamb, RD ;
Dalley, NK ;
Izatt, RM ;
Bradshaw, JS ;
Savage, PB .
TETRAHEDRON, 2004, 60 (49) :11139-11144
[10]   Quinoline-containing calixarene fluoroionophores: A combined NMR, photophysical and modeling study [J].
Casnati, A ;
Sansone, F ;
Sartori, A ;
Prodi, L ;
Montalti, M ;
Zaccheroni, N ;
Ugozzoli, F ;
Ungaro, R .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2003, 2003 (08) :1475-1485