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Protein Quantification by Derivatization-Free High-Performance Liquid Chromatography of Aromatic Amino Acids
Author(s) -
A. Hesse,
Michael G. Weller
Publication year - 2016
Publication title -
journal of amino acids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.188
H-Index - 5
eISSN - 2090-0112
pISSN - 2090-0104
DOI - 10.1155/2016/7374316
Subject(s) - derivatization , chromatography , phenylalanine , amino acid , aromatic amino acids , chemistry , detection limit , tryptophan , tyrosine , peptide , hydrolyzed protein , hydrolysis , bovine serum albumin , high performance liquid chromatography , biochemistry
Amino acid analysis is considered to be the gold standard for quantitative peptide and protein analysis. Here, we would like to propose a simple HPLC/UV method based on a reversed-phase separation of the aromatic amino acids tyrosine (Tyr), phenylalanine (Phe), and optionally tryptophan (Trp) without any derivatization. The hydrolysis of the proteins and peptides was performed by an accelerated microwave technique, which needs only 30 minutes. Two internal standard compounds, homotyrosine (HTyr) and 4-fluorophenylalanine (FPhe) were used for calibration. The limit of detection (LOD) was estimated to be 0.05 µ M (~10  µ g/L) for tyrosine and phenylalanine at 215 nm. The LOD for a protein determination was calculated to be below 16 mg/L (~300 ng BSA absolute). Aromatic amino acid analysis (AAAA) offers excellent accuracy and a precision of about 5% relative standard deviation, including the hydrolysis step. The method was validated with certified reference materials (CRM) of amino acids and of a pure protein (bovine serum albumin, BSA). AAAA can be used for the quantification of aromatic amino acids, isolated peptides or proteins, complex peptide or protein samples, such as serum or milk powder, and peptides or proteins immobilized on solid supports.

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