Time-Resolved Fluorescence Anisotropy Study of the Refolding Reaction of the α-Subunit of Tryptophan Synthase Reveals Nonmonotonic Behavior of the Rotational Correlation Time
| Autor: | Matthews Cr, Jill A. Zitzewitz, J. M. Beechem, Osman Bilsel, Li Yang |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Protein Folding
Time Factors biology Fluorescence Polarization Tryptophan synthase Biochemistry Anilino Naphthalenesulfonates Folding (chemistry) Kinetics chemistry.chemical_compound Crystallography Spectrometry Fluorescence Sulfonate Models Chemical chemistry Escherichia coli Tryptophan Synthase biology.protein Tyrosine Time-resolved spectroscopy Anisotropy Fluorescence anisotropy Rotational correlation time G alpha subunit |
| Zdroj: | Biochemistry. 38:4177-4187 |
| ISSN: | 1520-4995 0006-2960 |
| DOI: | 10.1021/bi9829433 |
| Popis: | Time-resolved fluorescence anisotropy of a bound extrinsic probe was studied in an effort to characterize dynamic properties of the transient partially folded forms that appear during the folding of the alpha-subunit of tryptophan synthase (alphaTS) from Escherichia coli. Previous studies have shown that alphaTS, a single structural domain, can be cleaved into autonomously folding amino- and carboxy-folding units comprising residues 1-188 and 189-268, respectively [Higgins, W., Fairwell, T., and Miles, E. W. (1979) Biochemistry 18, 4827-4835]. By use of a double-kinetic approach [Jones, B. E., Beechem, J. M., and Matthews, C. R. (1995) Biochemistry 34, 1867-1877], the rotational correlation time of 1-anilino-8-naphthalene sulfonate bound to nonpolar surfaces of folding intermediates was measured by time-correlated single photon counting at varying time delays following initiation of folding from the urea-denatured form by stopped-flow techniques. Comparison of the rotational correlation times for the full-length alphaTS and the amino-terminal fragment suggests that folding of the amino-terminal fragment and carboxy-terminal fragment is coordinated, not autonomous, on the milliseconds to seconds time scale. If a spherical shape is assumed, the apparent hydrodynamic radius of alphaTS after 5 ms is 26.8 A. The radius increases to 28.5 A by 1 s before decreasing to the radius for native alphaTS, 24.7 A, on a longer time scale (25 s). Viewed within the context of the kinetic folding model of alphaTS [Bilsel, O., Zitzewitz, J. A., Bowers, K. E. , and Matthews, C. R. (1999) Biochemistry 38, 1018-1029], the initial collapse reflects the formation of an off-pathway burst-phase intermediate in which at least part of the carboxy folding unit interacts with the amino folding unit. The subsequent increase in rotational correlation time corresponds to the formation of an on-pathway intermediate that leads to the native conformation. The apparent increase in the radius for the on-pathway intermediate may reflect a change in the interaction of the two-folding units, thereby forming a direct precursor for the alpha/beta barrel structure. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|