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Activation profile of cGMP-dependent protein kinase Iα
BMC Pharmacology and Toxicology volume 14, Article number: P79 (2013)
cGMP-dependent protein kinase (PKG) is a serine/threonine kinase which is potently activated by cGMP . PKG is encoded by two genes, forming two different proteins, PKGI and PKGII. The two isoforms of PKGI, PKGIα and PKGIβ, differ in the N-terminal amino acid sequences. PKGI isozymes are homodimers with two identical subunits possessing a catalytic and a regulatory domain each. The regulatory domain contains two non-identical binding sites for cyclic nucleotides (cNMPs), i.e., a slowly exchanging and a rapidly exchanging site. The activation constant (Ka) of PKGIα for cGMP is about 3-fold lower than the corresponding Ka of PKGIβ suggesting distinct physiological roles of the isoforms. In addition to cGMP, other cNMPs and also cNMP analogues activate or inhibit PKG [2–4]. While many investigations focussed on discrimination between the cNMP binding sites by employing cGMP and cAMP analogues, little is known about interaction of PKGIα with cCMP analogues or with Rp- and Sp- diastereomers of cCMP phosphorothioates.
As was shown by Desch et al. , the membrane-permeable cCMP analogue dibutyryl-cCMP (DB-cCMP) induces smooth muscle relaxation and activates PKGI in aortic tissue lysates. Therefore, we have studied 4-MB-cCMP, the resulting active metabolite after cleavage of DB-cCMP by esterases, and also corresponding substances from cAMP and cGMP, on purified PKGIα.
Materials and methods
PKG kinase activity was measured in-vitro by a radiometric kinase assay in the presence of cGMP or different cNMP analogues. pEC50 values, Ka, Hill slopes and Emax values were calculated using GraphPad Prism software. Emax values were related to Emax values of the activation of PKGIα by cGMP, which was set to 1.00.
Results and discussion
Besides the known activator cGMP, many other cNMPs and cNMP analogues are activators of PKGIα, with distinct activation constants (pEC50), specific Hill slopes and different maximal effects (Emax) (Table 1). The most potent and effective activator for PKGIα was cGMP. The active metabolite of DB-cGMP, 2-MB-cGMP was less potent and effective.
cAMP and 6-MB-cAMP showed similar potency, but 6-MB-cAMP had a higher efficacy than cAMP. 4-MB-cCMP was a more effective activator than cCMP, but showed a reduced potency.
The cNMP analogues activated PKGIα in the order of potency cGMP > 2-MB-cGMP > cAMP > 6-MB-cAMP > cCMP > 4-MB-cCMP and in the order of efficacy cGMP > 6-MB-cAMP > 4-MB-cCMP > 2-MB-cGMP > cAMP > cCMP.
Rp-cAMPS and Rp-cCMPS did not activate PKGIα. The stable phosphorothioates Sp-cAMPS and Sp-cCMPS activated PKGIα only at high concentrations in the order of potency and efficacy cGMP > cAMP > cCMP > Sp-cAMPS ~ Sp-cCMPS.
Furthermore, we illustrate binding of cNMPs for PKG based on existing crystal structures and discuss current problems with respect to molecular modelling approaches. In conclusion, 4-MB-cCMP is a more effective PKG activator than cCMP and, therefore, a valuable tool for analysing the second messenger role of cCMP .
Hofmann F: The biology of cyclic GMP-dependent protein kinases. J Biol Chem. 2005, 280: 1-4.
Corbin JD, Øgreid D, Miller JP, Suva RH, Jastorff B, Døskeland SO: Studies of cGMP analog specificity and function of the two intrasubunit binding sites of cGMP- dependent protein kinase. J Biol Chem. 1986, 261: 1208-1214.
Butt E, van Bemmelen M, Fischer L, Walter U, Jastorff B: Inhibition of cGMP- dependent protein kinase by (Rp)-guanosine 3′,5′-monophosphorothioates. FEBS Letters. 1990, 263: 47-50. 10.1016/0014-5793(90)80702-K.
Wolter S, Golombek M, Seifert R: Differential activation of cAMP- and cGMP- dependent protein kinases by cyclic purine and pyrimidine nucleotides. Biochem Biophys Res Commun. 2011, 415: 563-565. 10.1016/j.bbrc.2011.10.093.
Desch M, Schinner E, Kees F, Hofmann F, Seifert R, Schlossmann J: Cyclic cytidine 3′,5′-monophosphate (cCMP) signals via cGMP kinase I. FEBS Letters. 2010, 584: 3979-3984. 10.1016/j.febslet.2010.07.059.
Beste KY, Seifert R: cCMP, cUMP, cTMP, cIMP and cXMP as possible second messengers: development of a hypothesis based on studies with soluble guanyly l cyclase α1β2. Biol Chem. 2013, 394: 261-270.
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Wolter, S., Golombek, M., Schwede, F. et al. Activation profile of cGMP-dependent protein kinase Iα. BMC Pharmacol Toxicol 14, P79 (2013). https://0-doi-org.brum.beds.ac.uk/10.1186/2050-6511-14-S1-P79
- Active Metabolite
- Effective Activator
- Regulatory Domain
- GraphPad Prism Software
- Kinase Assay