| Literature DB >> 2500865 |
P Ostoa-Saloma1, J Ramírez, R Perez-Montfort.
Abstract
A qualitative and quantitative method to assay proteolytic degradation of casein with a spectrofluorometer was developed. Proteolysis produced by different pure or mixed proteinases in a pH range 2 to 7.4 quenches the fluorescence emitted at a wavelength of 350 nm by casein excited at 300 nm in less than 5 min. This method is very sensitive, fast, and requires minimal sample preparation. Proteinases that do not generate peptides appropriate for fluorescence quenching cannot be detected with this assay and proteinases with intrinsic fluorescence may require special adjustments of the spectrofluorometer. This method monitors the disappearance of intact substrate proteins continuously, omitting the separation step necessary in other methods to measure product peptides.Entities:
Mesh:
Substances:
Year: 1989 PMID: 2500865 DOI: 10.1016/0003-2697(89)90302-3
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365