Literature DB >> 3922238

Spectrophotometric estimation of protein concentration in the presence of tryptophan modified by 2-hydroxy-5-nitrobenzyl bromide.

E L Malin, R Greenberg, H M Farrell.   

Abstract

A spectrophotometric method makes it possible to determine the concentration of a protein after covalent modification of tryptophan residues by 2-hydroxy-5-nitrobenzyl bromide. Molar absorption coefficients for the 2-hydroxy-5-nitrobenzyl chromophore, reported here in the pH range from 4.0 to 10.9, can be used to correct the protein absorbance values at 280 nm, which then provides the basis for calculating protein concentration in the usual way. The method was tested with alpha-lactalbumin, beta-lactoglobulin, pepsin, and soybean trypsin inhibitor; spectrophotometrically estimated concentrations of these proteins agreed closely with values obtained by amino acid analysis.

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Year:  1985        PMID: 3922238     DOI: 10.1016/0003-2697(85)90128-9

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  Studies on the biotin-binding site of avidin. Tryptophan residues involved in the active site.

Authors:  G Gitlin; E A Bayer; M Wilchek
Journal:  Biochem J       Date:  1988-02-15       Impact factor: 3.857

2.  Modification of the mitochondrial F1-ATPase epsilon subunit, enhancement of the ATPase activity of the IF1-F1 complex and IF1-binding dependence of the conformation of the epsilon subunit.

Authors:  G Solaini; A Baracca; E Gabellieri; G Lenaz
Journal:  Biochem J       Date:  1997-10-15       Impact factor: 3.857

3.  Studies on the biotin-binding site of streptavidin. Tryptophan residues involved in the active site.

Authors:  G Gitlin; E A Bayer; M Wilchek
Journal:  Biochem J       Date:  1988-11-15       Impact factor: 3.857

  3 in total

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