Kinetic properties of DM-nitrophen and calcium indicators: rapid transient response to flash photolysis

被引:88
作者
Escobar, AL
Velez, P
Kim, AM
Cifuentes, F
Fill, M
Vergara, JL
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT PHYSIOL,LOS ANGELES,CA 90024
[2] INST VENEZOLANO INVEST CIENT,CTR BIOFIS & BIOQUIM,ALTOS DE PIPE,VENEZUELA
[3] LOYOLA UNIV,DEPT PHYSIOL,MAYWOOD,IL 60153
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1997年 / 434卷 / 05期
关键词
caged calcium; calcium indicators; flash photolysis; fluorescence transients; DM-nitrophen; kinetic modeling;
D O I
10.1007/s004240050444
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We describe a high temporal resolution confocal spot microfluorimetry setup which makes possible the detection of fluorescence transients elicited by Ca2+ indicators in response to large (50-200 mu M), short duration (<100 ns), free [Ca2+] transients generated by laser flash photolysis of DM-nitrophen (DM-n; caged Ca2+). The equilibrium and kinetic properties of the commercially available indicators Fluo-3, Rhod-2, CalciumOrange-5N (COr-5N) and CalciumGreen-2 (CGr-2) were determined experimentally. The data reveal that COr-5N displays simple, fast response kinetics while, in contrast, Fluo-3, Rhod-2 and CGr-2 are characterized by significantly slower kinetic properties. These latter indicators may be unsuitable for tracking Ca2+ signaling events lasting only a few milliseconds. A model which accurately predicts the time course of fluorescence transients in response to rapid free [Ca2+] changes was developed. Experimental data and model predictions concur only when the association rate constant of DM-n is approximately 20 times faster than previously reported. This work establishes a quantitative theoretical framework for the study of fast Ca2+ signaling events and the use of flash photolysis in cells and model systems.
引用
收藏
页码:615 / 631
页数:17
相关论文
共 40 条
  • [1] BIOLOGICALLY USEFUL CHELATORS THAT RELEASE CA-2+ UPON ILLUMINATION
    ADAMS, SR
    KAO, JPY
    GRYNKIEWICZ, G
    MINTA, A
    TSIEN, RY
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (10) : 3212 - 3220
  • [2] FREE CALCIUM-IONS IN NEURONS OF HELIX-ASPERSA MEASURED WITH ION-SELECTIVE MICROELECTRODES
    ALVAREZLEEFMANS, FJ
    RINK, TJ
    TSIEN, RY
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1981, 315 (JUN): : 531 - 548
  • [3] [Anonymous], 1990, CONFOCAL MICROSCOPY
  • [4] BERS DM, 1982, AM J PHYSIOL, V242, P404
  • [5] SPATIAL NONUNIFORMITIES IN [CA2+](I) DURING EXCITATION-CONTRACTION COUPLING IN CARDIAC MYOCYTES
    CANNELL, MB
    CHENG, H
    LEDERER, WJ
    [J]. BIOPHYSICAL JOURNAL, 1994, 67 (05) : 1942 - 1956
  • [6] Cifuentes F., 1995, Biophysical Journal, V68, pA419
  • [7] DELANEY KR, 1990, J PHYSIOL-LONDON, V4426, P473
  • [8] MEASUREMENTS OF INTRACELLULAR IONIZED CALCIUM IN SQUID GIANT-AXONS USING CALCIUM-SELECTIVE ELECTRODES
    DIPOLO, R
    ROJAS, H
    VERGARA, J
    LOPEZ, R
    CAPUTO, C
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 728 (03) : 311 - 318
  • [9] KINETICS OF CALCIUM-BINDING TO FLUO-3 DETERMINED BY STOPPED-FLOW FLUORESCENCE
    EBERHARD, M
    ERNE, P
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (01) : 309 - 314
  • [10] Laser photolysis of caged calcium: Rates of calcium release by nitrophenyl-EGTA and DM-nitrophen
    EllisDavies, GCR
    Kaplan, JH
    Barsotti, RJ
    [J]. BIOPHYSICAL JOURNAL, 1996, 70 (02) : 1006 - 1016