Site-specific dimensions across a highly denatured protein; a single molecule study

Evan R. McCarney, James H. Werner, Summer L. Bernstein, Ingo Ruczinski, Dmitrii E. Makarov, Peter M. Goodwin, Kevin W. Plaxco

Research output: Contribution to journalArticle

Abstract

Do highly denatured proteins adopt random coil configurations? Here, we address this question by measuring residue-to-residue separations across the denatured FynSH3 domain. Using single-molecule Forster resonance energy transfer techniques, we have collected transfer efficiency probability distributions for dye-labeled, denatured protein. Applying maximum likelihood analysis to the interpretation of these distributions, we have determined the through-space distance between five residue pairs in the protein's guanidine hydrochloride-unfolded and trifluoroethanol-unfolded states. We find that, while the dimensions of the guanidine hydrochloride -unfolded molecule generally coincide with the dimensions predicted for a random coil ensemble, potentially statistically significant deviations from random coil behavior are also evident. These small, site-specific deviations may provide a means of reconciling earlier, scattering-based evidence for the random coil nature of the unfolded state with more site-specific spectroscopic evidence suggesting residual structure. We have also studied the unfolded ensemble populated in 50% trifluoroethanol, a denaturant that induces a highly helical unfolded state. We find that the size and shape of the unfolded ensemble under these conditions is effectively indistinguishable from that populated in guanidinium hydrochloride solutions, suggesting that the gross structure of the denatured state is, perhaps surprisingly, independent of the chemistry of the cosolvent.

Original languageEnglish (US)
Pages (from-to)672-682
Number of pages11
JournalJournal of molecular biology
Volume352
Issue number3
DOIs
StatePublished - Sep 23 2005

Keywords

  • Denatured state
  • Lattice polymer simulations
  • Protein folding
  • Random coil
  • Single molecule

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

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  • Cite this

    McCarney, E. R., Werner, J. H., Bernstein, S. L., Ruczinski, I., Makarov, D. E., Goodwin, P. M., & Plaxco, K. W. (2005). Site-specific dimensions across a highly denatured protein; a single molecule study. Journal of molecular biology, 352(3), 672-682. https://doi.org/10.1016/j.jmb.2005.07.015