Previous Article | Next Article ![]()
Journal of Virology, May 1999, p. 4230-4238, Vol. 73, No. 5
Membrane Biology
Program1 and Nuclear Signalling
Laboratory,2 John Curtin School of Medical
Research, Australian National University, Canberra, ACT 2601, Australia
Received 29 June 1998/Accepted 19 February 1999
We have previously reported that the accessory protein Vpr from
human immunodeficiency virus type 1 forms cation-selective ion channels
in planar lipid bilayers and is able to depolarize intact cultured
neurons by causing an inward sodium current, resulting in cell death.
In this study, we used site-directed mutagenesis and synthetic peptides
to identify the structural regions responsible for the above functions.
Mutations in the N-terminal region of Vpr were found to affect channel
activity, whereas this activity was not affected by mutations in the
hydrophobic region of Vpr (amino acids 53 to 71). Analysis of mutants
containing changes in the basic C terminus confirmed previous results
that this region, although not necessary for ion channel function, was
responsible for the observed rectification of wild-type Vpr currents. A
peptide comprising the first 40 N-terminal amino acids of Vpr (N40) was found to be sufficient to form ion channels similar to those caused by
wild-type Vpr in planar lipid bilayers. Furthermore, N40 was able to
cause depolarization of the plasmalemma and cell death in cultured
hippocampal neurons with a time course similar to that seen with
wild-type Vpr, supporting the idea that this region is responsible for
Vpr ion channel function and cytotoxic effects. Since Vpr is found in
the serum and cerebrospinal fluids of AIDS patients, these results may
have significance for AIDS pathology.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The Amino-Terminal Region of Vpr from Human
Immunodeficiency Virus Type 1 Forms Ion Channels and Kills
Neurons

*
Corresponding author. Mailing address: Membrane Biology
Program, John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia. Phone: 612-6249-2759. Fax:
612-6249-0415. E-mail: Graeme.Cox{at}anu.edu.au.
Present address: Department of Microbiology, University of Alabama,
Birmingham, Ala.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»