Analysis of amino acid composition in proteins of animal tissues and foods as pre-column o-phthaldialdehyde derivatives by HPLC with fluorescence detection

被引:185
作者
Dai, Zhaolai [1 ]
Wu, Zhenlong [1 ]
Jia, Sichao [2 ,3 ]
Wu, Guoyao [1 ,2 ,3 ]
机构
[1] China Agr Univ, State Key Lab Anim Nutr, Beijing 100193, Peoples R China
[2] Texas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Med Physiol, College Stn, TX 77843 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2014年 / 964卷
基金
中国国家自然科学基金; 中国博士后科学基金; 美国食品与农业研究所;
关键词
Amino acids; HPLC; Hydrolysates; OPA (o-phthaldialdehyde); Proteins; PERFORMANCE LIQUID-CHROMATOGRAPHY; BOVINE BETA-CASEIN; PLUS HALF-CYSTINE; HYDROLYSIS METHOD; CYSTEINE RESIDUES; BASE HYDROLYSIS; BIOGENIC-AMINES; HUMAN-PLASMA; DERIVATIZATION; TRYPTOPHAN;
D O I
10.1016/j.jchromb.2014.03.025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Studies of protein nutrition and biochemistry require reliable methods for analysis of amino acid (AA) composition in polypeptides of animal tissues and foods. Proteins are hydrolyzed by 6M HCI (110 degrees C for 24h), 4.2M NaOH (105 degrees C for 20h), or proteases. Analytical techniques that require high-performance liquid chromatography (HPLC) include pre-column derivatization with 4-chloro-7-nitrobenzofurazan, 9-fluorenyl methylchloroformate, phenylisothiocyanate, naphthalene-2,3-dicarboxaldehyde, 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate, and o-phthaldialdehyde (OPA). OPA reacts with primary AA (except cysteine or cystine) in the presence of 2-mercaptoethanol or 3-mercaptopropionic acid to form a highly fluorescent adduct. OPA also reacts with 4-amino-1-butanol and 4-aminobutane-1,3-diol produced from oxidation of proline and 4-hydroxyproline, respectively, in the presence of chloramine-T plus sodium borohydride at 60 degrees C, or with S-carboxymethyl-cysteine formed from cysteine and iodoacetic acid at 25 degrees C. Fluorescence of OPA derivatives is monitored at excitation and emission wavelengths of 340 and 455 nm, respectively. Detection limits are 50 fmol for AA. This technique offers the following advantages: simple procedures for preparation of samples, reagents, and mobile-phase solutions; rapid pre-column formation of OPA-AA derivatives and their efficient separation at room temperature (e.g., 20-25 degrees C); high sensitivity of detection; easy automation on the HPLC apparatus; few interfering side reactions; a stable chromatography baseline for accurate integration of peak areas; and rapid regeneration of guard and analytical columns. Thus, the OPA method provides a useful tool to determine AA composition in proteins of animal tissues (e.g., skeletal muscle, liver, intestine, placenta, brain, and body homogenates) and foods (e.g., milk, corn grain, meat, and soybean meal). (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:116 / 127
页数:12
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