Ionic selectivity of low-affinity ratiometric calcium indicators: mag-Fura-2, Fura-2FF and BTC

被引:68
作者
Hyrc, KB [1 ]
Bownik, JM [1 ]
Goldberg, MP [1 ]
机构
[1] Washington Univ, Sch Med, Dept Neurol, Ctr Study Nervous Syst Injury, St Louis, MO 63110 USA
关键词
D O I
10.1054/ceca.1999.0092
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Accurate measurement of elevated intracellular calcium levels requires indicators with low calcium affinity and high selectivity. We examined fluorescence spectral properties and ionic specificity of three low-affinity, ratiometric indicators structurally related to Fura-2: mag-fura-2 (furaptra), Fura-2FF, and BTC. The indicators differed in respect to their excitation wavelengths, affinity for Ca2+ (K-d similar to 20 mu M, 6 mu M and 12 mu M respectively) and selectivity over Mg2(+) (K-d similar to 2 mM for mag-fura-2, >10 mM for Fura-2FF and ETC). Among the tested indicators, BTC was limited by a modest dynamic range upon Ca2+ binding, susceptibility to photodamage, and sensitivity to alterations in pH. All three indicators bound other metal ions including Zn2+, Cd2+ and Gd3+. Interestingly, only in the case of BTC were spectral differences apparent between Ca2+ and other metal ions. For example, the presence of Zn2+ increased BTC fluorescence 6-fold at the Ca2+ isosbestic point, suggesting that this dye may be used as a fluorescent Zn2+ indicator. Fura-2FF has high specificity, wide dynamic range, and low pH sensitivity, and is an optimal low-affinity Ca2+ indicator for most imaging applications. BTC may be useful if experimental conditions require visible wavelength excitation or sensitivity to other metal ions including Zn2+. (C) 2000 Harcourt Publishers Ltd.
引用
收藏
页码:75 / 86
页数:12
相关论文
共 73 条
[1]   CHARACTERIZATION OF N-(6-METHOXY-8-QUINOLYL)-P-TOLUENESULFONAMIDE FOR THE DETECTION OF ZINC IN LIVING SPERM CELLS [J].
ANDREWS, JC ;
NOLAN, JP ;
HAMMERSTEDT, RH ;
BAVISTER, BD .
CYTOMETRY, 1995, 21 (02) :153-159
[2]  
ARSLAN P, 1985, J BIOL CHEM, V260, P2719
[3]   MAGNETIC-RESONANCE SPECTROSCOPY STUDIES ON CA2+, ZN2+ AND ENERGY-METABOLISM IN SUPERFUSED BRAIN-SLICES [J].
BACHELARD, H ;
BADARGOFFER, R ;
MORRIS, P ;
THATCHER, N .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1994, 22 (04) :988-991
[4]   MICROSPECTROFLUOROMETRY AS A TOOL FOR INVESTIGATION OF NONCALCIUM INTERACTIONS OF INDO-1 [J].
BANCEL, F ;
SALMON, JM ;
VIGO, J ;
VIALLET, P .
CELL CALCIUM, 1992, 13 (01) :59-68
[5]   INVESTIGATION OF NONCALCIUM INTERACTIONS OF FURA-2 BY CLASSICAL AND SYNCHRONOUS FLUORESCENCE SPECTROSCOPY [J].
BANCEL, F ;
SALMON, JM ;
VIGO, J ;
VO-DINH, T ;
VIALLET, P .
ANALYTICAL BIOCHEMISTRY, 1992, 204 (02) :231-238
[6]   PHOTOBLEACHING OF FURA-2 AND ITS EFFECT ON DETERMINATION OF CALCIUM CONCENTRATIONS [J].
BECKER, PL ;
FAY, FS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (04) :C613-C618
[7]   The galvanization of biology: A growing appreciation for the roles of zinc [J].
Berg, JM ;
Shi, YG .
SCIENCE, 1996, 271 (5252) :1081-1085
[8]   Imaging free zinc in synaptic terminals in live hippocampal slices [J].
Budde, T ;
Minta, A ;
White, JA ;
Kay, AR .
NEUROSCIENCE, 1997, 79 (02) :347-358
[9]   GADOLINIUM AND NEOMYCIN BLOCK VOLTAGE-SENSITIVE CA2+ CHANNELS WITHOUT INTERFERING WITH THE NA+-CA2+ ANTIPORTER IN BRAIN NERVE-ENDINGS [J].
CANZONIERO, LMT ;
TAGLIALATELA, M ;
DIRENZO, G ;
ANNUNZIATO, L .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1993, 245 (02) :97-103
[10]   Measurement of intracellular free zinc in living neurons [J].
Canzoniero, LMT ;
Sensi, SL ;
Choi, DW .
NEUROBIOLOGY OF DISEASE, 1997, 4 (3-4) :275-279