Abstract
Nine different DNA enzymes (DzV3-n, n=1-9) targeting the V3 loop region of HIV-1 HXB2 were synthesized. One of those, DzV3-9, efficiently cleaved the target in the conserved sequence in the RNA transcript in vitro. DzV3-9 was stable in the cells and inhibited replication of both NL432 and SF162 strains in U87 cells expressing CD4 and co-receptors. The inhibitory effect of DNAzyme on incoming HIV-1 was also demonstrated with pseudotype virions generated by NL432-based luciferase reporter genes. Thus, an efficient, stable DNAzyme against a functionally important region of HIV-1 was identified, and it may be useful for prevention of HIV-1 infection.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antiviral Agents / chemical synthesis
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Antiviral Agents / pharmacology*
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Base Sequence
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Catalysis
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Cell Line
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DNA, Catalytic
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DNA, Single-Stranded / chemical synthesis
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DNA, Single-Stranded / pharmacology*
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DNA, Viral / chemical synthesis
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DNA, Viral / pharmacology*
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Enzyme Stability
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Gene Products, env / metabolism
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HIV Infections / enzymology
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HIV Infections / prevention & control
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HIV Infections / virology
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HIV-1 / drug effects*
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HIV-1 / pathogenicity
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HIV-1 / physiology
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Humans
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Hydrolysis
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Kinetics
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Molecular Sequence Data
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Peptide Fragments / metabolism
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RNA, Viral / metabolism*
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Virus Replication
Substances
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Antiviral Agents
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DNA, Catalytic
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DNA, Single-Stranded
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DNA, Viral
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Gene Products, env
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Peptide Fragments
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RNA, Viral