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PMID: 7578422 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Dissection of ADP-ribose polymer synthesis into individual steps of initiation, elongation, and branching.

Biochimie ·Vol. 77 ·No. 6 ·1995-00-00 ·Pages 403-7

Alvarez-Gonzalez R, Mendoza-Alvarez H

Abstract

We have studied the automodification reaction of poly(ADP-ribose)polymerase (PARP) (EC 2.4.2.30). The individual reactions of initiation, elongation, and branching catalyzed by this enzyme have been dissected out by manipulating the concentration of beta NAD, the ADP-ribosylation substrate. While PARP-mono(ADP-ribose) conjugates were the predominant products of automodification at 200 nM NAD (initiation), highly branched and complex polymers were synthesized at 200 microM NAD (polymerization). Initial rates of automodification increased with second order kinetics as a function of the enzyme concentration at both 200 nM and 200 microM NAD. These results are consistent with the conclusion that two molecules of PARP are required for ADP-ribose polymer synthesis during enzyme automodification. Thus, the auto-poly(ADP-ribosyl)ation reaction of PARP is intermolecular. In agreement with this notion, we observed that initial rates of the initiation reaction with 3'-deoxyNAD as a substrate also increased with the square of the enzyme concentration. In addition, the auto-poly(ADP-ribosyl)ation reaction of PARP increased with second order kinetics as a function of the NAD concentration at nanomolar levels (0.2-106 microM). Therefore, the dimeric structure of PARP also requires two molecules of bound NAD for efficient ADP-ribose polymerization.

MeSH Terms
Catalysis Kinetics Molecular Structure Peptide Chain Elongation, Translational Peptide Chain Initiation, Translational Poly Adenosine Diphosphate Ribose/biosynthesis,chemistry Poly(ADP-ribose) Polymerases/metabolism
Chemicals
Poly Adenosine Diphosphate Ribose Poly(ADP-ribose) Polymerases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Alvarez-Gonzalez R
Department of Microbiology and Immunology, University of North Texas Health Science Center at Fort Worth 76107-2699, USA.
Mendoza-Alvarez H
Article Info
Journal
Biochimie
Abbr.
Biochimie
ISSN
0300-9084
Published
1995-00-00
Pages
403-7
Language
English
Region
France
NLM ID
1264604
Subset
IM
Grants
NIGMS NIH HHS · GM45451 · United States
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