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Fluorescence studies of nucleotide interactions with bovine adrenal chromogranin A.
- Source :
-
Biochimica et biophysica acta [Biochim Biophys Acta] 1990 Aug 01; Vol. 1040 (1), pp. 66-70. - Publication Year :
- 1990
-
Abstract
- The binding of the fluorescent probe bis-ANS to chromogranin A, the major protein of adrenal chromaffin vesicles, caused a marked enhancement and blue shift in the fluorescence emission spectrum. The emission maximum shifted from 515 nm to 480 nm and the yield increased approx. 75-fold upon addition of 10 microM chromogranin A to 1 microM bis-ANS. Adenine nucleotides had clear effects on the bis-ANS fluorescence signal, while other nucleotides such as GTP, UTP and CTP had no discernible effect. Specifically, ATP caused a decrease in the fluorescence, whereas ADP and AMP caused a fluorescence increase. These results indicate adenine nucleotide binding to chromogranin A. Substitution of ATP with epsilon-ATP, an ATP derivative with a modification on the six-membered ring of the adenine base, failed to reduce the fluorescence intensity. Therefore, it was concluded that adenine bases play an important role in the chromogranin A-adenine nucleotide interaction.
- Subjects :
- Adenosine Triphosphate metabolism
Adrenal Medulla metabolism
Animals
Cattle
Chromaffin Granules metabolism
Chromogranin A
Chromogranins isolation & purification
Kinetics
Protein Binding
Spectrometry, Fluorescence methods
Chromogranins metabolism
Nerve Tissue Proteins metabolism
Ribonucleotides metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-3002
- Volume :
- 1040
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochimica et biophysica acta
- Publication Type :
- Academic Journal
- Accession number :
- 2378903
- Full Text :
- https://doi.org/10.1016/0167-4838(90)90146-7