The RelA nuclear localization signal folds upon binding to IκBα

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  • Carla F Cervantes, Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92092-0378, USA.
  • ,
  • Simon Bergqvist
  • ,
  • Magnus Kjærgaard
  • Gerard Kroon
  • ,
  • Shih-Che Sue
  • ,
  • H Jane Dyson
  • ,
  • Elizabeth A Komives
The nuclear localization signal (NLS) polypeptide of RelA, the canonical nuclear factor-κB family member, is responsible for regulating the nuclear localization of RelA-containing nuclear factor-κB dimers. The RelA NLS polypeptide also plays a crucial role in mediating the high affinity and specificity of the interaction of RelA-containing dimers with the inhibitor IκBα, forming two helical motifs according to the published X-ray crystal structure. In order to define the nature of the interaction between the RelA NLS and IκBα under solution conditions, we conducted NMR and isothermal titration calorimetry studies using a truncated form of IκBα containing residues 67-206 and a peptide spanning residues 293-321 of RelA. The NLS peptide, although largely unfolded, has a weak tendency toward helical structure when free in solution. Upon addition of the labeled peptide to unlabeled IκBα, the resonance dispersion in the NMR spectrum is significantly greater, providing definitive evidence that the RelA NLS polypeptide folds upon binding IκBα. Isothermal titration calorimetry studies of single-point mutants reveal that residue F309, which is located in the middle of the more C-terminal of the two helices (helix 4) in the IκBα-bound RelA NLS polypeptide, is critical for the binding of the RelA NLS polypeptide to IκBα. These results help to explain the role of helix 4 in mediating the high affinity of RelA for IκBα.
Original languageEnglish
JournalJournal of Molecular Biology
Volume405
Issue3
Pages (from-to)754-64
Number of pages11
ISSN0022-2836
DOIs
Publication statusPublished - 21 Jan 2011
Externally publishedYes

    Research areas

  • Amino Acid Motifs, Amino Acid Sequence, Animals, Cell Nucleus, Humans, I-kappa B Proteins, Models, Molecular, Molecular Sequence Data, Nuclear Localization Signals, Protein Binding, Protein Folding, Protein Multimerization, Protein Structure, Secondary, Transcription Factor RelA

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