Effect of oxidative stress on in vivo ADP-ribosylation of eukaryotic elongation factor 2


Bektas M. , Akcakaya H., Aroymak A., Nurten R., Bermek E.

INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, vol.37, no.1, pp.91-99, 2005 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 37 Issue: 1
  • Publication Date: 2005
  • Doi Number: 10.1016/j.biocel.2004.05.016
  • Title of Journal : INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
  • Page Numbers: pp.91-99

Abstract

Different lines of evidence indicate that eukaryotic elongation factor 2 (eEF2) can be ADP-ribosylated endogenously. The physiological significance of this reaction has, however, remained unclarified. In order to address this issue we investigated the in vivo ADP-ribosylation of eEF2 and the effect of oxidative stress thereon. The investigation revealed that the endogenous ADP-ribosylation of eEF2 is complex and can take place in K562 cell lysates either under the action of endogenous transferase from [adenosine-C-14]NAD or by direct binding of free [C-14]ADP-ribose. These two types of ADP-ribosylation were distinguished by use of different treatments based on the chemical stability of the respective bonds formed. Under standard culture conditions, in vivo labeling of eEF2 in the presence of [C-14]adenosine was reversed to about 65% in the presence of diphtheria toxin and nicotinamide. This finding implied that the modification that took place under physiological circumstances was, mainly, of an enzymic nature. On the other hand, H2O2-promoted oxidative stress gave rise to a nearly two-fold increase in the extent of in vivo labeling of eEF2. This was accompanied by a loss of eEF2 activity in polypeptide chain elongation. Oxidative stress specifically inhibited the subsequent binding of free ADP-ribose to eEF2. The results thus provide evidence that endogenous ADP-ribosylation of eEF2 can also take place by the binding of free ADP-ribose. This nonenzymic reaction appears to account primarily for in vivo ADP-ribosylation of eEF2 under oxidative stress. (C) 2004 Elsevier Ltd. All rights reserved.