Duplex unwinding and ATPase activities of the DEAD-box helicase eIF4A are coupled by eIF4G and eIF4B

J Mol Biol. 2011 Sep 30;412(4):674-87. doi: 10.1016/j.jmb.2011.08.004. Epub 2011 Aug 5.

Abstract

Eukaryotic initiation factor (eIF) 4A is a DEAD-box helicase that stimulates translation initiation by unwinding mRNA secondary structure. The accessory proteins eIF4G, eIF4B, and eIF4H enhance the duplex unwinding activity of eIF4A, but the extent to which they modulate eIF4A activity is poorly understood. Here, we use real-time fluorescence assays to determine the kinetic parameters of duplex unwinding and ATP hydrolysis by these initiation factors. To ensure efficient duplex unwinding, eIF4B and eIF4G cooperatively activate the duplex unwinding activity of eIF4A. Our data reveal that eIF4H is much less efficient at stimulating eIF4A unwinding activity than eIF4B, implying that eIF4H is not able to completely substitute for eIF4B in duplex unwinding. By monitoring unwinding and ATPase assays under identical conditions, we demonstrate that eIF4B couples the ATP hydrolysis cycle of eIF4A with strand separation, thereby minimizing nonproductive unwinding events. Using duplex substrates with altered GC contents but similar predicted thermal stabilities, we further show that the rate of formation of productive unwinding complexes is strongly influenced by the local stability per base pair, in addition to the stability of the entire duplex. This finding explains how a change in the GC content of a hairpin is able to influence translation initiation while maintaining the overall predicted thermal stability.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Adenosine Triphosphatases / physiology
  • Base Composition / physiology
  • Base Pairing / physiology
  • DEAD-box RNA Helicases / chemistry
  • DEAD-box RNA Helicases / metabolism
  • DNA Helicases / metabolism*
  • DNA Helicases / physiology
  • Enzyme Activation / physiology
  • Eukaryotic Initiation Factor-4A / chemistry
  • Eukaryotic Initiation Factor-4A / metabolism*
  • Eukaryotic Initiation Factor-4G / chemistry
  • Eukaryotic Initiation Factor-4G / metabolism
  • Eukaryotic Initiation Factor-4G / physiology*
  • Eukaryotic Initiation Factors / chemistry
  • Eukaryotic Initiation Factors / metabolism
  • Eukaryotic Initiation Factors / physiology*
  • Humans
  • Hydrolysis
  • Models, Biological
  • Models, Molecular
  • Nucleic Acid Heteroduplexes / chemistry
  • Nucleic Acid Heteroduplexes / metabolism*
  • Protein Structure, Tertiary

Substances

  • EIF4G1 protein, human
  • Eukaryotic Initiation Factor-4G
  • Eukaryotic Initiation Factors
  • Nucleic Acid Heteroduplexes
  • eIF-4B
  • Eukaryotic Initiation Factor-4A
  • Adenosine Triphosphatases
  • DNA Helicases
  • DEAD-box RNA Helicases