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To elucidate the kinetic importance of structural intermediates in single-domain proteins, we measured the effect of solution conditions and amino-acid changes at a central core residue of ubiquitin (Val 26) on the kinetics of folding and unfolding. Kinetic analysis in terms of a sequential three-state mechanism provides insight into the contribution of specific interactions within the ubiquitin core to the structural stability of the native and intermediate states. The observations that disruptive mutations and/or addition of denaturants result in an apparent two-state folding process with slower rates is explained by the destabilization of a partially folded intermediate, which is in rapid equilibrium with unfolded states. The model predicts that under sufficiently stabilizing conditions kinetic intermediates may become populated even for proteins showing apparent two-state kinetics.

More information Original publication

DOI

10.1038/nsb0296-193

Type

Journal article

Publication Date

1996-02-01T00:00:00+00:00

Volume

3

Pages

193 - 205

Total pages

12

Addresses

I, n, s, t, i, t, u, t, e, , f, o, r, , C, a, n, c, e, r, , R, e, s, e, a, r, c, h, ,, , F, o, x, , C, h, a, s, e, , C, a, n, c, e, r, , C, e, n, t, e, r, ,, , P, h, i, l, a, d, e, l, p, h, i, a, ,, , P, e, n, n, s, y, l, v, a, n, i, a, , 1, 9, 1, 1, 1, ,, , U, S, A, .

Keywords

Humans, Valine, Ubiquitins, Spectrometry, Fluorescence, Protein Denaturation, Protein Folding, Kinetics, Mutation, Models, Chemical, Models, Molecular