Cholesterol Modulates the Interaction between HIV-1 Viral Protein R and Membrane

• Published in: Membranes (Basel) Vol. 11; no. 10; p. 784
• Main Authors: Liu, Chun-Hao, Huang, Shing-Jong, Yu, Tsyr-Yan
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 13-10-2021; MDPI
• Subjects: Amino acids; Calcein; calcein release; Carbonyl compounds; Carbonyls; Cell cycle; Cellular structure; Chloride; Cholesterol; E coli; HIV; HIV-1; Homeostasis; Human immunodeficiency virus; Infectivity; Life cycles; Line shape; lipid composition; Lipids; membrane; Membrane permeability; Membrane proteins; Membranes; Metabolites; Molecular weight; NMR; Nuclear magnetic resonance; Peptides; Permeability; Proteins; Sodium; Spectroscopy; Spectrum analysis; Viruses; Vpr; Vpr protein; St Louis Missouri; United Kingdom > UK; United States > US; HIV-1; NMR; membrane; REDOR; Vpr; calcein release; cholesterol; lipid composition
• ISSN: 2077-0375; 2077-0375
• DOI: 10.3390/membranes11100784

Being a major metabolite for maintaining cellular homeostasis, as well as an important structural component in lipid membrane, cholesterol also plays critical roles in the life cycles of some viruses, including human immunodeficiency virus-1 (HIV-1). The involvement of cholesterol in HIV-1 infectivity, assembly and budding has made it an important research target. Viral protein R (Vpr) is an accessory protein of HIV-1, which is involved in many major events in the life cycle of HIV-1. In addition to its multi-functional roles in the HIV-1 life cycle, it is shown to interact with lipid membrane and form a cation-selective channel. In this work, we examined the effect of cholesterol on the interaction of Vpr and lipid membrane. Using calcein release assay, we found that the membrane permeability induced by the membrane binding of Vpr was significantly reduced in the presence of cholesterol in membrane. In addition, using solid-state NMR (ssNMR) spectroscopy, Vpr was shown to experience multiple chemical environments in lipid membrane, as indicated by the broad line shape of carbonyl
C resonance of Cys-76 residue ranging from 165-178 ppm, which can be attributed to the existence of complex Vpr-membrane environments. We further showed that the presence of cholesterol in membrane will alter the distribution of Vpr in the complex membrane environments, which may explain the change of the Vpr induced membrane permeability in the presence of cholesterol.