Literature DB >> 15617

Application of trinitrophenylation for the measurement of alpha-amino residues resulting from peptic digestion.

M T Yuko, K Hotta.   

Abstract

A sensitive and precise method for the measurement of peptic activity on protein substrate is described. alpha-Amino residues formed by pepsin digestion are photometrically measured by comparing the absorbances of digested and nondigested material which has been trinitrophenylated. The usual problem of high reagent-blank absorbance is eliminated by using an anion exchange resin, Dowex 1-X8. In contrast to Anson's method, the procedure requires only 1/100 the quantity of protein substrate for analysis. It was proved to be particularly useful for the estimation of initial rates of proteolysis.

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Year:  1977        PMID: 15617     DOI: 10.1016/0005-2744(77)90296-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  2 in total

1.  Interplay of PDZ and protease domain of DegP ensures efficient elimination of misfolded proteins.

Authors:  Tobias Krojer; Karen Pangerl; Juliane Kurt; Justyna Sawa; Christoph Stingl; Karl Mechtler; Robert Huber; Michael Ehrmann; Tim Clausen
Journal:  Proc Natl Acad Sci U S A       Date:  2008-05-27       Impact factor: 11.205

2.  Impact of Helicobacter pylori colonization on immunoreactive epidermal growth factor and transforming growth factor-alpha in gastric juice. Its potential pathogenetic implications.

Authors:  M Marcinkiewicz; B Van Der Linden; D A Peura; G Goldin; S Parolisi; J Sarosiek
Journal:  Dig Dis Sci       Date:  1996-11       Impact factor: 3.199

  2 in total

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