4.5 Article

Studies on the reversible enzyme reaction of rabbit muscle glycogen phosphorylase b using isothermal titration calorimetry

Journal

CARBOHYDRATE RESEARCH
Volume 477, Issue -, Pages 58-65

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carres.2019.03.014

Keywords

Glycogen phosphorylase; Isothermal titration calorimetry; Reversible enzyme reaction; Substrate inhibition; Activity measurement

Funding

  1. EU
  2. European Regional Development Fund [GINOP-2.3.2-15-2016-00008]
  3. ITC [TAMOP-4.2.1.-15-B-09/1/KONV]
  4. OTKA [CK77515]

Ask authors/readers for more resources

Glycogen phosphorylase enzymes (GP) catalyse reversible reactions; the glucose transfer from glycogen to inorganic phosphate (P-i, phosphorolysis) or the reverse glucose transfer from glucose-l-phosphate (G-1-P) to glycogen (synthesis). Rabbit muscle GPb (rmGPb) was used as a model enzyme to study the reversible enzyme reaction. To follow both directions of this reversible reaction, we have developed a novel isothermal titration calorimetry (ITC) method for the determination of the direct reaction rate. The preference of forward or reverse reaction was ensured by the 0.1 or 10 concentration ratios of G-1-P/P-i, respectively. Substrate specificity was studied using different maltooligosaccharides and glycogen. Based on the K-M values, glycogen and 2-chloro-4-nitrophenyl maltoheptaoside (CNP-G7) were found to be analogous substrates, which allowed to optimize the method by taking advantage of the CNP chromophore being detectable in HPLC. In case of CNP-G7, substrate inhibition was observed and characterised by K-i of 23 +/- 7 mM. Inhibition of human GP is a promising strategy for the treatment of diabetes. Our ITC measurements have confirmed that caffeine and glucopyranosylidenespiro-thiohydantoin (GTH), as known GPb inhibitors, inhibit the rmGPb-catalysed reversible reaction in both directions. K-i values obtained in the direction of synthesis (1.92 +/- 0.14 mM for caffeine and 11.5 +/- 2.0 p.M for GTH) have been shown to be in good agreement with the K-i values obtained in the direction of phosphorolysis (4.05 +/- 0.26 mM for caffeine and 13.8 +/- 1.6 mu M for GTH). The higher difference between the inhibition constants of caffeine was explained by the non-competitive mechanism. The described ITC method using the developed experimental design and reaction conditions is suitable for activity measurements of different phosphorylase enzymes on various substrates and is applicable for inhibition studies as well.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available