ANTI-(HUMAN IMMUNODEFICIENCY VIRUS) ACTIVITY OF POLYOXOTUNGSTATES AND THEIR INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE

被引:19
作者
MOORE, PS
JONES, CJ
MAHMOOD, N
EVANS, IG
GOFF, M
COOPER, R
HAY, AJ
机构
[1] MRC,CTR COLLABORAT,LONDON NW7 1AD,ENGLAND
[2] UNIV BIRMINGHAM,SCH CHEM,BIRMINGHAM B15 2TT,W MIDLANDS,ENGLAND
[3] UNIV MANCHESTER,DEPT PATHOL SCI,DIV VIROL,MANCHESTER M13 9PT,LANCS,ENGLAND
[4] MRC,DIV VIROL,LONDON NW7 1AA,ENGLAND
关键词
D O I
10.1042/bj3070129
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:129 / 134
页数:6
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