Chemical and physiological characterization of fluo-4 Ca2+-indicator dyes

被引:462
作者
Gee, KR [1 ]
Brown, KA [1 ]
Chen, WNU [1 ]
Bishop-Stewart, J [1 ]
Gray, D [1 ]
Johnson, I [1 ]
机构
[1] Mol Probes Inc, Eugene, OR 97402 USA
关键词
D O I
10.1054/ceca.1999.0095
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have developed fluo-4, a new fluorescent dye for quantifying cellular Ca2+ concentrations in the 100 nM to 1 mu M range. Fluo-4 is similar in structure and spectral properties to the widely used fluorescent Ca2+-indicator dye, fluo-3, but it has certain advantages over fluo-3. Due to its greater absorption near 488 nm, fluo-4 offers substantially brighter fluorescence emission when used with excitation by argon-ion laser or other sources in conjunction with the standard fluorescein filter set. In vitro, fluo-4 exhibited high fluorescence emission, a high rate of cell permeation, and a large dynamic range for reporting [Ca2+] around a K-d(Ca2+) of 345 nM. We have also developed several Ca2+-indicators related to fluo-4 having lower affinities for Ca2+ that are useful in cellular studies requiring quantification of higher [Ca2+]. In a variety of physiological studies of live cells, fluo-4 labeled cells more brightly than did fluo-3, when challenged with procedures designed to elevate calcium levels. Fluo-4 is well suited for photometric and imaging applications that make use of confocal laser scanning microscopy, flow cytometry, or spectrofluorometry, or in fluorometric high-throughput microplate screening assays. Because of its higher fluorescence emission intensity, fluo-4 can be used at lower intracellular concentrations, making its use a less invasive practice. (C) 2000 Harcourt Publishers Ltd.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 35 条
[1]   Time-resolved monitoring of electrogenic Na+-Ca2+ exchange in the isolated cardiac sarcolemma vesicles by using a rapid-response fluorescent probe [J].
Baazov, D ;
Wang, XL ;
Khananshvili, D .
BIOCHEMISTRY, 1999, 38 (05) :1435-1445
[2]   Regulation of Ca2+ transport by sarcoplasmic reticulum Ca2+-ATPase at limiting [Ca2+] [J].
Berman, MC .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1418 (01) :48-60
[3]   SPATIAL NONUNIFORMITIES IN [CA2+](I) DURING EXCITATION-CONTRACTION COUPLING IN CARDIAC MYOCYTES [J].
CANNELL, MB ;
CHENG, H ;
LEDERER, WJ .
BIOPHYSICAL JOURNAL, 1994, 67 (05) :1942-1956
[4]   Chimeric G proteins allow a high-throughput signaling assay of Gi-coupled receptors [J].
Coward, P ;
Chan, SDH ;
Wada, HG ;
Humphries, GM ;
Conklin, BR .
ANALYTICAL BIOCHEMISTRY, 1999, 270 (02) :242-248
[5]   Nuclear versus perinuclear and cytoplasmic calcium in osteoclasts [J].
Ferrier, J ;
Yu, H .
CELL CALCIUM, 1996, 20 (05) :381-388
[6]   Calcium buffering capacity of neuronal cell cytosol measured by flash photolysis of calcium buffer NP-EGTA [J].
Fleet, A ;
Ellis-Davies, G ;
Bolsover, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (03) :786-790
[7]   Endogenous buffers limit the spread of free calcium in hair cells [J].
Hall, JD ;
Betarbet, S ;
Jaramillo, F .
BIOPHYSICAL JOURNAL, 1997, 73 (03) :1243-1252
[8]   CYTOSOLIC CA2+ OSCILLATIONS IN REF52 FIBROBLASTS - CA2+-STIMULATED IP3 PRODUCTION OR VOLTAGE-DEPENDENT CA2+ CHANNELS AS KEY POSITIVE FEEDBACK ELEMENTS [J].
HAROOTUNIAN, AT ;
KAO, JPY ;
PARANJAPE, S ;
ADAMS, SR ;
POTTER, BVL ;
TSIEN, RY .
CELL CALCIUM, 1991, 12 (2-3) :153-164
[9]  
HAUGLAND RP, 1996, HDB FLUORESCENT PROB, P505
[10]   THAPSIGARGIN-INDUCED NUCLEAR CALCIUM SIGNALS IN RAT BASOPHILIC LEUKEMIA-CELLS [J].
HORIKOSHI, Y ;
FURUNO, T ;
TESHIMA, R ;
SAWADA, J ;
NAKANISHI, M .
BIOCHEMICAL JOURNAL, 1994, 304 :57-60