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Examples
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Using an in-vitro integration assay system, we show that these peptides, namely INr-1 and INr-2, abrogate inhibition of integrase activity by the Rev protein as well as by the Rev-derived peptides.
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INr > HIV-1; (B) INr > Rev peptide > HIV-1; (C) Rev peptide > HIV-1 > INr; (D) INr >
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INr peptides stimulate HIV-infection of LC5-RIC cultures.
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The complex was then incubated with either one or both of the INr peptides at the designated Rev-GFP: peptide ratio.
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Fig 8A and B demonstrate that the reverse transcription step was not effected by the addition of the INr peptides.
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Inhibition of IN enzymatic activity by Rev and its abrogation by the INr peptides.
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Stimulation of viral DNA integration events by the INr peptides.
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On the other hand, the INr peptides failed to abrogate the inhibitory effects of two LEDGF derived peptides
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Furthermore both INr peptides enhanced virus infection in three different assay systems.
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Our results clearly show that incubation with the INr peptides stimulate viral DNA integration leading to multiple integration events.
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