Anti-(human immunodeficiency virus) activity of polyoxotungstates and their inhibition of human immunodeficiency virus reverse transcriptase

Author:

Moore P S1,Jones C J2,Mahmood N1,Evans I G2,Goff M3,Cooper R3,Hay A J4

Affiliation:

1. Medical Research Council, Collaborative Centre, 1-3 Burtonhole Lane, Mill Hill, London NW7 1AD, U.K.

2. School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.

3. Department of Pathological Sciences, Division of Virology, University of Manchester, Stopford Building, Oxford Road, Manchester M13 9PT, U.K.

4. Medical Research Council, Division of Virology, The Ridgeway, Mill Hill, London NW7 1AA, U.K.

Abstract

Heteropolyoxotungstates of the Keggin class containing different heteroatoms were tested for inhibition of two strains of human immunodeficiency virus 1 (HIV-1); they exhibited varying antiviral activity. Compounds containing boron were inactive, only one of those containing phosphorus showed selective anti-viral activity, whereas all silicon-containing compounds exhibited significant anti-viral activity in C8166 cells infected with the IIIB strain. Their effectiveness was some 10-fold higher in JM cells with selectivity indices of about 2000. The silicotungstates were effective inhibitors of HIV reverse transcriptase, showing greater inhibition with RNA/DNA template primers than with DNA/DNA template.primer. Kinetic analysis demonstrated that they inhibit the enzyme by different mechanisms, as, of the four compounds examined, two competed with template.primer and two competed with deoxynucleoside triphosphate. Inhibition of DNA polymerase activity by these compounds was compared using polymerases from different sources, including human; although not necessarily most specific for HIV-1 reverse transcriptase, they did not inhibit all DNA polymerases to a similar degree.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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