Publication | Closed Access
Enzyme-Friendly, Mass Spectrometry-Compatible Surfactant for In-Solution Enzymatic Digestion of Proteins
314
Citations
16
References
2003
Year
Mass Spectrometry-compatible SurfactantEnzymatic ModificationProtein PurificationBioanalysisBiochemical EngineeringAnalytical ChemistryClinical ChemistryProteomicsChromatographyProtein ChemistryBiochemistryPharmacologyTrypsin ActivityBiomolecular EngineeringPeptide CoverageNatural SciencesPeptide LibraryMass SpectrometryProtein Mass SpectrometryEnzyme SpecificityProtein EngineeringMedicine
Improved in-solution tryptic digestion of proteins in terms of speed and peptide coverage was achieved with the aid of a novel acid-labile anionic surfactant (ALS). Unlike SDS, ALS solubilizes proteins without inhibiting trypsin or other common endopeptidases activity. Trypsin activity was evaluated in the presence of various denaturants; little or no decrease in proteolytic activity was observed in 0.1-1% ALS solutions (w/v). Sample preparation prior to mass spectrometry and liquid chromatography analysis consists of sample acidification. ALS degrades rapidly at low-pH conditions, which eliminates surfactant-caused interference with analysis. Described methodology combines the advantages of protein solubilization, rapid digestion, high peptide coverages, and easy sample preparation for mass spectrometry and liquid chromatography analyses.
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