Literature DB >> 17012324

Enzyme kinetics above denaturation temperature: a temperature-jump/stopped-flow apparatus.

Bálint Kintses1, Zoltán Simon, Máté Gyimesi, Júlia Tóth, Balázs Jelinek, Csaba Niedetzky, Mihály Kovács, András Málnási-Csizmadia.   

Abstract

We constructed a "temperature-jump/stopped-flow" apparatus that allows us to study fast enzyme reactions at extremely high temperatures. This apparatus is a redesigned stopped-flow which is capable of mixing the reactants on a submillisecond timescale concomitant with a temperature-jump even as large as 60 degrees C. We show that enzyme reactions that are faster than the denaturation process can be investigated above denaturation temperatures. In addition, the temperature-jump/stopped-flow enables us to investigate at physiological temperature the mechanisms of many human enzymes, which was impossible until now because of their heat instability. Furthermore, this technique is extremely useful in studying the progress of heat-induced protein unfolding. The temperature-jump/stopped-flow method combined with the application of structure-specific fluorescence signals provides novel opportunities to study the stability of certain regions of enzymes and identify the unfolding-initiating regions of proteins. The temperature-jump/stopped-flow technique may become a breakthrough in exploring new features of enzymes and the mechanism of unfolding processes.

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Year:  2006        PMID: 17012324      PMCID: PMC1779911          DOI: 10.1529/biophysj.106.092833

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  12 in total

1.  Resolution of conformational states of Dictyostelium myosin II motor domain using tryptophan (W501) mutants: implications for the open-closed transition identified by crystallography.

Authors:  A Málnási-Csizmadia; R J Woolley; C R Bagshaw
Journal:  Biochemistry       Date:  2000-12-26       Impact factor: 3.162

2.  Kinetic resolution of a conformational transition and the ATP hydrolysis step using relaxation methods with a Dictyostelium myosin II mutant containing a single tryptophan residue.

Authors:  A Málnási-Csizmadia; D S Pearson; M Kovács; R J Woolley; M A Geeves; C R Bagshaw
Journal:  Biochemistry       Date:  2001-10-23       Impact factor: 3.162

3.  The dynamics of the relay loop tryptophan residue in the Dictyostelium myosin motor domain and the origin of spectroscopic signals.

Authors:  A Malnasi-Csizmadia; M Kovacs; R J Woolley; S W Botchway; C R Bagshaw
Journal:  J Biol Chem       Date:  2001-02-22       Impact factor: 5.157

4.  Folding at the speed limit.

Authors:  Wei Yuan Yang; Martin Gruebele
Journal:  Nature       Date:  2003-05-08       Impact factor: 49.962

5.  A "slow" temperature jump apparatus built from a stopped-flow machine.

Authors:  W H Goldmann; M A Geeves
Journal:  Anal Biochem       Date:  1991-01       Impact factor: 3.365

6.  ATPase kinetics of the Dictyostelium discoideum myosin II motor domain.

Authors:  P A Kuhlman; C R Bagshaw
Journal:  J Muscle Res Cell Motil       Date:  1998-06       Impact factor: 2.698

7.  Differential scanning calorimetric study of the thermal unfolding of the motor domain fragments of Dictyostelium discoideum myosin II.

Authors:  D I Levitsky; M A Ponomarev; M A Geeves; V L Shnyrov; D J Manstein
Journal:  Eur J Biochem       Date:  1998-01-15

8.  A simple stopped-flow temperature-jump apparatus.

Authors:  A S Verkman; J A Dix; A A Pandiscio
Journal:  Anal Biochem       Date:  1981-10       Impact factor: 3.365

9.  Myosin cleft movement and its coupling to actomyosin dissociation.

Authors:  Paul B Conibear; Clive R Bagshaw; Piotr G Fajer; Mihály Kovács; András Málnási-Csizmadia
Journal:  Nat Struct Biol       Date:  2003-09-21

10.  Overexpression of myosin motor domains in Dictyostelium: screening of transformants and purification of the affinity tagged protein.

Authors:  D J Manstein; D M Hunt
Journal:  J Muscle Res Cell Motil       Date:  1995-06       Impact factor: 2.698

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