Glyceraldehyde-3-phosphate Dehydrogenase and Nm23-H1/Nucleoside Diphosphate Kinase A

Matthias Engel, Markus Seifert, Birgit Theisinger, Ulrich Seyfert, Cornelius Welter
1998 Journal of Biological Chemistry  
We have recently discovered an alternative function of the putative metastasis suppressor protein Nm23, which is identical to nucleoside diphosphate kinase, as a protein phosphotransferase in vitro. While purified native Nm23 protein did not phosphorylate other proteins, we could purify a Nm23-associated protein that activates the protein phosphotransferase function; it was identified as a glyceraldehyde-3-phosphate dehydrogenase (GAPDH) isoenzyme. Co-expression and purification of (His) 6
more » ... ed GAPDH in combination with either Nm23-H1 or Nm23-H2 in baculovirus-infected Sf9 cells showed that only Nm23-H1, but not Nm23-H2, forms a stable complex with GAPDH. Protein phosphotransferase activity was confirmed for the recombinant GAPDH⅐Nm23-H1 complex but not for either of the enzymes alone, nor was this activity observed after simple mixing of the purified proteins in vitro. The molecular mass of the highly purified recombinant GAPDH⅐ Nm23-H1 complex suggests that a dimer of GAPDH interacts with a dimer of Nm23-H1. In contrast to the complex with GAPDH, co-expression of Nm23-H1 with antioxidant protein (MER-5) or creatine kinase did not activate the protein phosphotransferase function, indicating that this activation may specifically require GAPDH as a binding partner. 1 The abbreviations used are: NDP, nucleoside diphosphate; Awd k-pn , Awd killer of prune; (d)NTP, (deoxy)nucleoside triphosphate; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; DTT, dithiothreitol; PAGE, polyacrylamide gel electrophoresis; PCR, polymerase chain reaction.
doi:10.1074/jbc.273.32.20058 pmid:9685345 fatcat:rbimcz3refebrmgafevkddxnva