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PMID: 1692732 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mechanism of HIV reverse transcriptase: enzyme-primer interaction as revealed through studies of a dNTP analogue, 3'-azido-dTTP.

Biochemistry ·Vol. 29 ·No. 15 ·1990-04-17 ·Pages 3603-11

Kedar PS, Abbotts J, Kovács T, Lesiak K, Torrence P, Wilson SH

Abstract

Primer and dNTP recognition by purified HIV reverse transcriptase have been investigated. Earlier kinetic studies suggested that the reaction pathway for DNA synthesis is ordered, with template-primer and free enzyme combining to form the first complex in the reaction sequence [Majumdar et al. (1988) J. Biol. Chem. 263, 15657-15665], and through use of a particularly high affinity template-primer analogue [r(I)n.Sd(C)28], rate values for formation of the first complex were calculated [Majumdar et al. (1989) Biochemistry 28, 1340-1346]. We now report rate values for first complex formation in the usual model replication system with poly[r(A)].oligo [d(T)] as template-primer. We find that 3'-azido-dTTP (AZTTP) is a linear competitive inhibitor of DNA synthesis against the substrate dNTP (dTTP) in the poly[r(A)].oligo[d(T)] replication system. This suggests that 3'-azido-dTTP and dTTP combine with the same form of the enzyme in the reaction scheme, i.e., the enzyme-primer complex. This is not trivial, since a second analogue, 3'-amino-dTTP, also is an inhibitor against dTTP, but the mechanism in this case is linear noncompetitive. Because the inhibition by 3'-azido-dTTP is linear competitive, the KD for physical binding to the enzyme is assumed to be the same as the Ki for inhibition (20 nM). Substrate kinetic studies of DNA synthesis using 3'-azido-dTTP as substrate revealed that the Michaelis constant is 3 microM. Therefore, the Km for this substrate analogue is 100-fold higher than the KD for binding of the analogue to the enzyme-primer complex.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Antiviral Agents Bacteriophages/genetics Chemical Phenomena Chemistry DNA/biosynthesis DNA-Directed DNA Polymerase/genetics,metabolism Dideoxynucleotides HIV/enzymology Kinetics Models, Molecular RNA-Directed DNA Polymerase/genetics,metabolism Templates, Genetic Thymine Nucleotides/metabolism Zidovudine/analogs & derivatives,metabolism
Chemicals
Antiviral Agents Dideoxynucleotides Thymine Nucleotides Zidovudine zidovudine triphosphate DNA RNA-Directed DNA Polymerase DNA-Directed DNA Polymerase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kedar P S
Laboratory of Biochemistry, National Cancer Institute, Bethesda, Maryland 20892.
Abbotts J
Kovács T
Lesiak K
Torrence P
Wilson S H
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1990-04-17
Pages
3603-11
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Corrections
ErratumIn
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