Literature DB >> 420776

Melting-profile analysis of thermal stability of thermolysin. A formulation of temperature-scanning kinetics.

S C Fujita, N Go, K Imahori.   

Abstract

The melting-profile method consists of a continuous observation of a structural parameter while the temperature of the sample is raised at a constant rate [Fugita, S. C., & Imahori, K. (1974) IN Peptides, Polypeptides and Proteins (Blout, E. R., Bovey, F. A., Goodman, M., & Lotan, N., Eds.) p 217, Wiley, New York, N.Y.]. An analytical solution to the melting profile was formulated for the two-state irreversible process and called temperature-scanning kinetics. The theory was tested with thermolysin with consistent results, and the thermodynamic parameters of thermal denaturation were calculated: deltaH identical to = 80.3 kcal/mol, deltaS identical to = 153 eu. These values agreed with the corresponding values obtained from the classical constant-temperature relaxation kinetics. The possibilities of temperature-scanning kinetics are discussed.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 420776     DOI: 10.1021/bi00568a004

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  2 in total

1.  A statistical mechanical deconvolution of the differential scanning calorimetric profiles of the thermal denaturation of cyanomethemoglobin.

Authors:  Shahrokh Safarian; Masoud Alimohammadi; Abbas Ali Saberi; Ali Akbar Moosavi-Movahedi
Journal:  Protein J       Date:  2005-04       Impact factor: 2.371

2.  The relative conformational stability of the alcohol dehydrogenase alleloenzymes of the fruitfly Drosophila melanogaster.

Authors:  D R Thatcher; R Sheikh
Journal:  Biochem J       Date:  1981-07-01       Impact factor: 3.857

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.