Literature DB >> 5288248

The sequential unfolding of ribonuclease A: detection of a fast initial phase in the kinetics of unfolding.

T Y Tsong, R L Baldwin, E L Elson.   

Abstract

Temperature-jump studies have been used to detect a rapid reaction in the thermal unfolding of ribonuclease A (RNase A). The fast reaction occurs over a wide range of pH, and the results of a detailed study at pH 1.3 are reported here. Although its amplitude is small, the reaction is easily measurable over the entire temperature range of thermal unfolding. It occurs in the millisecond time range, and is faster by 3-4 orders of magnitude than the slow unfolding reaction studied previously. Unfolding is measured here by the change in absorbance at 287 nm, which reflects the exposure to solvent of buried tyrosine groups. Since the fast reaction has a detectable amplitude only in the temperature range of unfolding, it apparently detects the presence of intermediate, partly-folded states. Previous equilibrium studies of the unfolding of RNase A in the pH range 1-2 have indicated that it is essentially a 2-state reaction, without detectable intermediates. The existence of a rapid transient phase in the unfolding of RNase A had been predicted previously from a model for this unfolding reaction, based on nucleation-dependent sequential folding. The model served to reconcile kinetic and equilibrium studies of the thermal unfolding reaction of RNase A at neutral pH. Kinetic studies had shown that the slow unfolding reaction, measured at 287 nm, could be represented as a single exponential process, as expected for a 2-state reaction. However, earlier equilibrium measurements, especially the calorimetric studies of Sturtevant and coworkers, had revealed significant deviations from the 2-state behavior at neutral pH. These conflicting observations are explained by the model, which satisfies closely many criteria for a 2-state unfolding, even when appreciable concentrations of partly folded molecules are present. In particular, it predicts that the final, and major, portion of the kinetic reaction will occur as a single process characterized by an exponential time course.

Entities:  

Mesh:

Substances:

Year:  1971        PMID: 5288248      PMCID: PMC389507          DOI: 10.1073/pnas.68.11.2712

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  12 in total

1.  Evidence for the instability of hydrogen-bonded peptide structures in water, based on studies of ribonuclease and oxidized ribonuclease.

Authors:  W F HARRINGTON; J A SCHELLMAN
Journal:  C R Trav Lab Carlsberg Chim       Date:  1956

2.  Kinetic evidence for incorrectly folded intermediate states in the refolding of denatured proteins.

Authors:  A Ikai; C Tanford
Journal:  Nature       Date:  1971-03-12       Impact factor: 49.962

Review 3.  Protein denaturation.

Authors:  C Tanford
Journal:  Adv Protein Chem       Date:  1968

4.  [A simple temperature range method in the seconds to hours range and the reversible denaturation of chymotrypsin].

Authors:  F M Pohl
Journal:  Eur J Biochem       Date:  1968-04

5.  Kinetics of folding of staphylococcal nuclease.

Authors:  A N Schechter; R F Chen; C B Anfinsen
Journal:  Science       Date:  1970-02-06       Impact factor: 47.728

6.  A calorimetric study of thermally induced conformational transitions of ribonuclease A and certain of its derivatives.

Authors:  T Y Tsong; R P Hearn; D P Wrathall; J M Sturtevant
Journal:  Biochemistry       Date:  1970-06-23       Impact factor: 3.162

7.  Thermal effects on the circular dichroism spectra of ribonuclease A and of ribonuclease S-protein.

Authors:  E R Simons; E G Schneider; E R Blout
Journal:  J Biol Chem       Date:  1969-08-10       Impact factor: 5.157

8.  Validity of the "two-state" hypothesis for conformational transitions of proteins.

Authors:  R Lumry; R Biltonen
Journal:  Biopolymers       Date:  1966-09       Impact factor: 2.505

9.  Evidence for residual structure in acid- and heat-denatured proteins.

Authors:  K C Aune; A Salahuddin; M H Zarlengo; C Tanford
Journal:  J Biol Chem       Date:  1967-10-10       Impact factor: 5.157

10.  The thermodynamics of protein denaturation. 3. The denaturation of ribonuclease in water and in aqueous urea and aqueous ethanol mixtures.

Authors:  J F Brandts; L Hunt
Journal:  J Am Chem Soc       Date:  1967-09-13       Impact factor: 15.419

View more
  14 in total

1.  Fast-folding protein kinetics, hidden intermediates, and the sequential stabilization model.

Authors:  S Banu Ozkan; Ken A Dill; Ivet Bahar
Journal:  Protein Sci       Date:  2002-08       Impact factor: 6.725

2.  Cooperativity in two-state protein folding kinetics.

Authors:  Thomas R Weikl; Matteo Palassini; Ken A Dill
Journal:  Protein Sci       Date:  2004-03       Impact factor: 6.725

3.  Quantitative study of polymer conformation and dynamics by single-particle tracking.

Authors:  H Qian; E L Elson
Journal:  Biophys J       Date:  1999-03       Impact factor: 4.033

4.  Network representation of conformational transitions between hidden intermediates of Rd-apocytochrome b562.

Authors:  Mojie Duan; Hanzhong Liu; Minghai Li; Shuanghong Huo
Journal:  J Chem Phys       Date:  2015-10-07       Impact factor: 3.488

5.  An IMS-IMS threshold method for semi-quantitative determination of activation barriers: Interconversion of proline cis↔trans forms in triply protonated bradykinin.

Authors:  Nicholas A Pierson; David E Clemmer
Journal:  Int J Mass Spectrom       Date:  2015-02-01       Impact factor: 1.986

6.  Protein folding: are we there yet?

Authors:  A Clay Clark
Journal:  Arch Biochem Biophys       Date:  2008-01-01       Impact factor: 4.013

7.  Protein folding: then and now.

Authors:  Yiwen Chen; Feng Ding; Huifen Nie; Adrian W Serohijos; Shantanu Sharma; Kyle C Wilcox; Shuangye Yin; Nikolay V Dokholyan
Journal:  Arch Biochem Biophys       Date:  2007-06-08       Impact factor: 4.013

8.  Protein folding: matching theory and experiment.

Authors:  D V Laurents; R L Baldwin
Journal:  Biophys J       Date:  1998-07       Impact factor: 4.033

9.  Transition paths, diffusive processes, and preequilibria of protein folding.

Authors:  Zhuqing Zhang; Hue Sun Chan
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-03       Impact factor: 11.205

Review 10.  An emerging concept of prion infections as a form of transmissible cerebral amyloidosis.

Authors:  Omar Lupi; Marcius Achiame Peryassu
Journal:  Prion       Date:  2007 Oct-Dec       Impact factor: 3.931

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.