Abstract
Cyclic PNAs targeting the HIV-1 TAR RNA loop have been synthesized following a convenient solid-phase strategy which allows on-resin cyclisation. UV-monitored thermal denaturation studies demonstrate that these cyclic PNAs are able to strongly interact with their TAR RNA target, very likely through the formation of a six-base pair stable complex, involving the TAR RNA loop.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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HIV-1 / genetics*
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Peptide Nucleic Acids / chemical synthesis*
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Peptide Nucleic Acids / chemistry
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Peptide Nucleic Acids / pharmacology
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Peptides, Cyclic / chemical synthesis*
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Peptides, Cyclic / chemistry
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Peptides, Cyclic / pharmacology
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RNA, Viral / drug effects*
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Spectrophotometry, Ultraviolet
Substances
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Peptide Nucleic Acids
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Peptides, Cyclic
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RNA, Viral