Format

Send to

Choose Destination
J Biol Chem. 2018 Dec 7;293(49):18828-18840. doi: 10.1074/jbc.RA118.003944. Epub 2018 Oct 11.

Structural basis for targeting avian sarcoma virus Gag polyprotein to the plasma membrane for virus assembly.

Author information

1
From the Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294 and.
2
the Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York 11794.
3
From the Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294 and saad@uab.edu.

Abstract

For most retroviruses, including HIV-1, binding of the Gag polyprotein to the plasma membrane (PM) is mediated by interactions between Gag's N-terminal myristoylated matrix (MA) domain and phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) in the PM. The Gag protein of avian sarcoma virus (ASV) lacks the N-myristoylation signal but contains structural domains having functions similar to those of HIV-1 Gag. The molecular mechanism by which ASV Gag binds to the PM is incompletely understood. Here, we employed NMR techniques to elucidate the molecular determinants of the membrane-binding domain of ASV MA (MA87) to lipids and liposomes. We report that MA87 binds to the polar head of phosphoinositides such as PI(4,5)P2 We found that MA87 binding to inositol phosphates (IPs) is significantly enhanced by increasing the number of phosphate groups, indicating that the MA87-IP binding is governed by charge-charge interactions. Using a sensitive NMR-based liposome-binding assay, we show that binding of MA87 to liposomes is enhanced by incorporation of PI(4,5)P2 and phosphatidylserine. We also show that membrane binding is mediated by a basic surface formed by Lys-6, Lys-13, Lys-23, and Lys-24. Substitution of these residues to glutamate abolished binding of MA87 to both IPs and liposomes. In an accompanying paper, we further report that mutation of these lysine residues diminishes Gag assembly on the PM and inhibits ASV particle release. These findings provide a molecular basis for ASV Gag binding to the inner leaflet of the PM and advance our understanding of the basic mechanisms of retroviral assembly.

KEYWORDS:

ASV; Gag protein; avian sarcoma virus; human immunodeficiency virus (HIV); inositol hexakisphosphate; isothermal titration calorimetry (ITC); liposome; myristoylated matrix; phosphatidylinositol 4,5-bisphosphate; phosphatidylserine; plasma membrane

PMID:
30309983
PMCID:
PMC6295720
[Available on 2019-12-07]
DOI:
10.1074/jbc.RA118.003944

Supplemental Content

Full text links

Icon for HighWire
Loading ...
Support Center