Literature DB >> 528637

Titration curves of polypeptide chains by combined isoelectric focusing-electrophoresis in 8 M urea.

P G Righetti, F Krishnamoorthy, C Lapoumeroulie, D Labie.   

Abstract

Titration curves of reduced and alkylated polypeptide chains can be successfully performed in 8 M urea-polyacrylamide gel plates by electrophoresis perpendicular to a stationary stack of focused carrier ampholytes. All buffers and thiol reagents with pK values in the range pH 3--10 should be removed, since their pH-dependent ionization affects the migration and apparent pI values of the protein chains. No blurring of the patterns below pH 4.5 is observed, as usually found in titration curves in the absence of urea, thus allowing the direct titration of Glu and Asp residues. It is not possible by the present technique to titrate any group below pH ca. 3 and above pH ca. 10, due to the lack of suitable carrier ampholytes and to a "flooding" phenomenon, with concomitant identical electrophoretic mobility for all protein species, irrespective of their relative pI values and amino acid composition. The "electrophoretic titration curves" thus obtained were well correlated with the overall amino acid composition of the polypeptide chains analyzed.

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Year:  1979        PMID: 528637     DOI: 10.1016/s0021-9673(01)96317-4

Source DB:  PubMed          Journal:  J Chromatogr


  2 in total

1.  A novel approach to study of the structural basis of enzyme polymorphism. Analysis of carboxylesterase B of Escherichia coli as model.

Authors:  B Picard; P Goullet; R Krishnamoorthy
Journal:  Biochem J       Date:  1987-02-01       Impact factor: 3.857

2.  An analysis of molecular polymorphism of esterase M produced by motile Aeromonas strains.

Authors:  B Picard; J C Philippe; P Goullet
Journal:  Biochem Genet       Date:  1990-02       Impact factor: 1.890

  2 in total

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