Cyclic Nucleotide Phosphodiesterases from Rat Pancreas: Differential Regulation by a Calcium-Dependent Activator Protein

1977 ◽  
Vol 5 (4) ◽  
pp. 981-982 ◽  
Author(s):  
ANDRE VANDERMEERS ◽  
M. CLAIRE VANDERMEERS ◽  
JEAN RATHE ◽  
ALAIN DELFORGE ◽  
JEAN CHRISTOPHE
1995 ◽  
Vol 25 (2) ◽  
pp. 235A
Author(s):  
Roland R. Brandt ◽  
Holger Heinrich ◽  
Claudia C.S. Chini ◽  
Lawrence L. Aarhus ◽  
Thomas P. Dousa ◽  
...  

1979 ◽  
Vol 28 (8) ◽  
pp. 1307-1312 ◽  
Author(s):  
Richard G. van Inwegen ◽  
Phyllis Salaman ◽  
Vassil St. Georgiev ◽  
Ira Weinryb

2002 ◽  
Vol 7 (3) ◽  
pp. 215-222 ◽  
Author(s):  
Wei Huang ◽  
Yan Zhang ◽  
J. Richard Sportsman

Cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of the 3′-ester bond of cyclic AMP (cAMP) and cyclic GMP (cGMP), important second messengers in the transduction of a variety of extracellular signals. There is growing interest in the study of PDEs as drug targets for novel therapeutics. We describe the development of a homogeneous fluorescence polarization assay for PDEs based on the strong binding of PDE reaction products (i.e., AMP or GMP) onto modified nanoparticles through interactions with immobilized trivalent metal cations. This assay technology (IMAP) is applicable to both cAMP- and cGMP-specific PDEs. Results of the assay in 384- and 1536-well microplates are presented.


2004 ◽  
Vol 483 (2-3) ◽  
pp. 187-194 ◽  
Author(s):  
Chin-Chung Wu ◽  
Wei-Ya Wang ◽  
Reen-Yen Kuo ◽  
Fang-Rong Chang ◽  
Yang-Chang Wu

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