Abstract
In HIV-1 reverse transcription, the nucleocapsid protein, NC, induces secondary structure fluctuations in specific DNA and RNA hairpins. Time-resolved single-molecule fluorescence resonance energy transfer was used to study NC chaperoned opening of DNA hairpins over a broader range of conditions and in more depth than in previous studies. The experiments reveal a complex mechanism for secondary structure fluctuations with dynamic processes occurring over a wide time range, i.e., approximately 5 to >250 ms and with the involvement of long-lived intermediates. The dynamic role of DNA loop regions and NC binding/dissociation events are discussed.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Base Sequence
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Binding Sites
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DNA / chemistry*
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DNA / genetics
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DNA / metabolism
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Fluorescence Resonance Energy Transfer / methods
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HIV-1 / chemistry
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HIV-1 / genetics
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HIV-1 / metabolism
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Kinetics
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Molecular Chaperones / chemistry*
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Molecular Chaperones / genetics
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Molecular Chaperones / metabolism
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Nucleic Acid Conformation
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Nucleocapsid Proteins / chemistry*
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Nucleocapsid Proteins / genetics
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Nucleocapsid Proteins / metabolism
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RNA / chemistry
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RNA / genetics
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RNA / metabolism
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Reverse Transcription*
Substances
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Molecular Chaperones
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Nucleocapsid Proteins
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RNA
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DNA