Purification and characterization of two initiation factors required for maximal activity of a highly fractionated globin mRNA translation system

Proc Natl Acad Sci U S A. 1976 Aug;73(8):2584-8. doi: 10.1073/pnas.73.8.2584.

Abstract

Two additional initiation factors (IF-M4 and IF-M5) have been purified and characterized both physically and biologically. IF-M4 is active as a single polypeptide chain with a molecular weight of 48,000. In contrast, IF-M5 is active as a complex with a molecular weight of about 500,000 and consists of seven major and several minor polypeptide components. Analysis of IF-M5 in two polyacrylamide gel electrophoresis systems indicated that one of the major polypeptide chains of IF-M5 was the 35,000 dalton subunit of IF-MP. This analysis also revealed that IF-M2A, IF-M3, and elongation factor 2 were present as minor components. Both IF-M4 and IF-M5 are required to achieve maximal activity in an assay system dependent on exogenous globin mRNA, but neither factor has been observed to stimulate model reactions that utilize artificial templates [poly(U) or AUG].

MeSH terms

  • Animals
  • Cell-Free System
  • Globins
  • Molecular Weight
  • Peptide Elongation Factors / analysis
  • Peptide Initiation Factors / analysis
  • Peptide Initiation Factors / isolation & purification*
  • Poly U / metabolism
  • Protein Biosynthesis*
  • RNA, Messenger / metabolism*
  • Rabbits
  • Reticulocytes
  • Ribonucleoproteins / analysis

Substances

  • Peptide Elongation Factors
  • Peptide Initiation Factors
  • RNA, Messenger
  • Ribonucleoproteins
  • Poly U
  • Globins