Dengue virus NS4A cytoplasmic domain binding to liposomes is sensitive to membrane curvature

Biochim Biophys Acta. 2015 May;1848(5):1119-26. doi: 10.1016/j.bbamem.2015.01.015. Epub 2015 Jan 30.

Abstract

Dengue virus (DENV) infection is a growing public health threat with more than one-third of the world's population at risk. Non-structural protein 4A (NS4A), one of the least characterized viral proteins, is a highly hydrophobic transmembrane protein thought to induce the membrane alterations that harbor the viral replication complex. The NS4A N-terminal (amino acids 1-48), has been proposed to contain an amphipathic α-helix (AH). Mutations (L6E; M10E) designed to reduce the amphipathic character of the predicted AH, abolished viral replication and reduced NS4A oligomerization. Nuclear magnetic resonance (NMR) spectroscopy was used to characterize the N-terminal cytoplasmic region (amino acids 1-48) of both wild type and mutant NS4A in the presence of SDS micelles. Binding of the two N-terminal NS4A peptides to liposomes was studied as a function of membrane curvature and lipid composition. The NS4A N-terminal was found to contain two AHs separated by a non-helical linker. The above mentioned mutations did not significantly affect the helical secondary structure of this domain. However, they reduced the affinity of the N-terminal NS4A domain for lipid membranes. Binding of wild type NS4A(1-48) to liposomes is highly dependent on membrane curvature.

Keywords: Amphipathic helix; Curvature sensing; Dengue virus; NMR spectroscopy; Non-structural protein NS4A; Peptide membrane interaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circular Dichroism
  • Dengue Virus / growth & development
  • Dengue Virus / metabolism*
  • Liposomes
  • Membrane Lipids / chemistry
  • Membrane Lipids / metabolism*
  • Micelles
  • Mutation
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Binding
  • Protein Multimerization
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Structure-Activity Relationship
  • Surface Plasmon Resonance
  • Viral Nonstructural Proteins / chemistry
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / metabolism*
  • Virus Replication

Substances

  • Liposomes
  • Membrane Lipids
  • Micelles
  • NS4A protein, Dengue virus
  • Viral Nonstructural Proteins