Evidence for non-two-state kinetics in the nucleocapsid protein chaperoned opening of DNA hairpins

J Phys Chem B. 2006 Feb 9;110(5):2419-26. doi: 10.1021/jp054189i.

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

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Base Sequence
  • Binding Sites
  • DNA / chemistry*
  • DNA / genetics
  • DNA / metabolism
  • Fluorescence Resonance Energy Transfer / methods
  • HIV-1 / chemistry
  • HIV-1 / genetics
  • HIV-1 / metabolism
  • Kinetics
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Nucleic Acid Conformation
  • Nucleocapsid Proteins / chemistry*
  • Nucleocapsid Proteins / genetics
  • Nucleocapsid Proteins / metabolism
  • RNA / chemistry
  • RNA / genetics
  • RNA / metabolism
  • Reverse Transcription*

Substances

  • Molecular Chaperones
  • Nucleocapsid Proteins
  • RNA
  • DNA