The nitrodibenzofuran chromophore: a new caging group for ultra-efficient photolysis in living cells

被引:182
作者
Momotake, A
Lindegger, N
Niggli, E
Barsotti, RJ
Ellis-Davies, GCR
机构
[1] Drexel Univ, Coll Med, Dept Physiol & Pharmacol, Philadelphia, PA 19102 USA
[2] Univ Bern, Dept Physiol, CH-3012 Bern, Switzerland
[3] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
关键词
D O I
10.1038/NMETH821
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Photochemical uncaging of bio-active molecules was introduced in 1977, but since then, there has been no substantial improvement in the properties of generic caging chromophores. We have developed a new chromophore, nitrodibenzofuran (NDBF) for ultra-efficient uncaging of second messengers inside cells. Photolysis of a NDBF derivative of EGTA (caged calcium) is about 16-160 times more efficient than photolysis of the most widely used caged compounds (the quantum yield of photolysis is 0.7 and the extinction coefficient is 18,400 M-1 cm(-1)). Ultraviolet (UV)-laser phototysis of NDBF-EGTA:Ca2+ rapidly released Ca2+ (rate of 20,000 s(-1)) and initiated contraction of skinned guinea pig cardiac muscle. NDBF-EGTA has a two-photon cross-section of similar to 0.6 GM and two-photon phototysis induced localized Ca2+-induced Ca2+ release from the sarcoplasmic recticulum of intact cardiac myocytes. Thus, the NDBF chromophore has great promise as a generic and photochemically efficient protecting group for both one- and two-photon uncaging in living cells.
引用
收藏
页码:35 / 40
页数:6
相关论文
共 30 条
[1]  
Adams D.F., 1967, Journal of Composite Materials, V1, P4, DOI [10.1177/002199836700100102, DOI 10.1177/002199836700100102]
[2]   BIOLOGICALLY USEFUL CHELATORS THAT RELEASE CA-2+ UPON ILLUMINATION [J].
ADAMS, SR ;
KAO, JPY ;
GRYNKIEWICZ, G ;
MINTA, A ;
TSIEN, RY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (10) :3212-3220
[3]  
BALTROP JA, 1996, J CHEM SOC CHEM COMM, P822
[4]  
Brown E B, 1998, Methods Enzymol, V291, P356
[5]   Photolysis of caged calcium in femtoliter volumes using two-photon excitation [J].
Brown, EB ;
Shear, JB ;
Adams, SR ;
Tsien, RY ;
Webb, WW .
BIOPHYSICAL JOURNAL, 1999, 76 (01) :489-499
[6]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[7]   Photon upmanship: Why multiphoton imaging is more than a gimmick [J].
Denk, W ;
Svoboda, K .
NEURON, 1997, 18 (03) :351-357
[8]   Synthesis of photosensitive EGTA derivatives [J].
Ellis-Davies, GCR .
TETRAHEDRON LETTERS, 1998, 39 (09) :953-956
[9]  
Ellis-Davies GCR, 2003, METHOD ENZYMOL, V360, P226
[10]  
ELLISDAVIES GC, 2005, IMAGING NEUROSCIENCE, P367