Transmembrane movement and distribution of cholesterol in the membrane of vesicular stomatitis virus

• Published in: Biochemistry (Easton) Vol. 17; no. 20; pp. 4192 - 4200
• Main Authors: Patzer, Eric J., Shaw, J. Michael, Moore, Norman F., Thompson, Thomas E., Wagner, Robert R.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01.10.1978
• Subjects: Cell Line; Cholesterol - physiology; Kinetics; Membrane Lipids - physiology; Phospholipids - physiology; Vesicular stomatitis Indiana virus - physiology
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00613a013

The transmembrane movement and distribution of cholesterol in the vesicular stomatitis virus membrane were studied by following the depletion of cholesterol from virions to interacting phospholipid vesicles and by exchange of radiolabeled cholesterol between virions and phospholipid-cholesterol vesicles. The kinetics of the cholesterol exchange or depletion reactions revealed the presence of two exponential rates: a rapid rate, dependent on the vesicle to virus ratio, and a slower rate, independent of the vesicle to virus ratio. The kinetics of cholesterol movement could be best interpreted by a model of the virion membrane considered as a two pool system in which approximately 30% of the cholesterol resides in the outer monolayer and approximately 70% in the inner monolayer. The half-time for equilibration of the two pools was calculated to be 4--6 h and was assumed to represent the time required for transmembrane movement of cholesterol across the bilayer. The initial rate of transfer of cholesterol from virus into vesicles increased when vesicle phospholipids contained more unsaturated and shorter chain fatty acids. Furthermore, the transfer of cholesterol appeared to occur by a collisional mechanism requiring membrane-membrane contact. Interaction with lipid vesicles did not significantly affect the integrity of the virion membrane as assessed by the relative inaccessibility of internal proteins to lactoperoxidase-catalyzed iodination and by the small loss of [3H]amino acid labeled protein from the virus.