Adrenaline specifically increases the phosphorylation of cardiac troponin I at serine-20 in the perfused rabbit heart.
Answers are grounded in this paper and cite their sources.
Adrenaline may modulate myofilament function via Ser-20 phosphorylation in rabbit hearts; leaves open its role and relevance in human cardiac disease.
On treatment of the perfused rabbit heart with adrenaline, the total covalently bound phosphate of troponin I increased from 1.14 mol of phosphate/mol to 1.86 mol of phosphate/mol. 2. Covalently bound phosphate could be identified only in the region of the molecule of cardiac troponin I consisting of residues 1--48. 3. When 32P-labelled orthophosphate was present in the perfusion medium the phosphate at serine-20 became radioactively labelled. This residue was the only significant site of phosphorylation that could be identified. 4. The addition of adrenaline caused a 4--5-fold increase in covalently bound [32P]phosphate. Virtually all of the 32P was located at serine-20. 5. It was concluded from these studies that the extent of phosphorylation of serine-20 of cardiac troponin I increased from 30--40% in the control perfused heart to about 100% in the presence of adrenaline.
No takes yet. Share an insight, caveat, or question.
Moir et al. (1980) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: