Potential of capillary electrophoresis for the monitoring of the stability of placental alkaline phosphatase

被引:8
作者
Eriksson, HJC
Wijngaard, M
Hinrichs, WLJ
Frijlink, HW
Somsen, GW
de Jong, GJ
机构
[1] Univ Groningen, Dept Pharmaceut Anal, NL-9713 AV Groningen, Netherlands
[2] Univ Groningen, Dept Pharmaceut Technol & Biopharm, NL-9713 AV Groningen, Netherlands
关键词
alkaline phosphatase; therapeutic protein; protein stability; capillary electrophoresis; enzymatic activity;
D O I
10.1016/S0731-7085(02)00646-5
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Alkaline phosphatase (AP) is a potential therapeutic agent in the treatment of sepsis. In this paper the potential of capillary zone electrophoresis (CZE) for the monitoring of the degradation of placental alkaline phosphatase (PLAP) was investigated. To induce degradation PLAP samples were exposed to high temperatures, low and high pH and freeze-drying. The samples were then analyzed by CZE and enzymatic activity assay. Upon exposure to temperatures above 65 degreesC, PLAP lost its activity exponentially over time, while CZE revealed both a linear decrease of the area of the main peak and a rise of degradation products. At acidic pH the enzyme appeared to lose its activity. CZE revealed a decrease of the area of the main peak, but no degradation products could be detected. At pH 12 the enzymatic activity and the area of the main peak both decreased linearly over time and, in addition, formation of degradation products could be detected by CZE. Activity and CZE profile of PLAP remained unchanged upon freeze-drying in the presence of inulin. Prolonged storage of freeze-dried samples at room temperature caused a slight decrease of enzymatic activity, while the potential formation of oligomers was revealed by CZE analysis. The examples in this study show that, in combination with activity assays, CZE can provide useful complementary information, especially on the status of the protein and the presence of degradation products. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:351 / 357
页数:7
相关论文
共 20 条
[1]   THE THERMAL-DENATURATION OF STEM BROMELAIN IS CONSISTENT WITH AN IRREVERSIBLE 2-STATE MODEL [J].
ARROYOREYNA, A ;
HERNANDEZARANA, A .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1995, 1248 (02) :123-128
[2]  
DAIHO T, 1994, J BIOL CHEM, V269, P11060
[3]   INTERDOMAIN INTERACTIONS IN THE CHIMERIC PROTEIN TOXIN SCD4(178)-PE40 - A DIFFERENTIAL SCANNING CALORIMETRY (DSC) STUDY [J].
DAVIO, SR ;
KIENLE, KM ;
COLLINS, BE .
PHARMACEUTICAL RESEARCH, 1995, 12 (05) :642-648
[4]  
EICHLER J, 1994, J BIOL CHEM, V269, P30093
[5]   Characterization of human placental alkaline phosphatase by activity and protein assays, capillary electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [J].
Eriksson, HJC ;
Somsen, GW ;
Hinrichs, WLJ ;
Frijlink, HW ;
de Jong, GJ .
JOURNAL OF CHROMATOGRAPHY B, 2001, 755 (1-2) :311-319
[6]   HUMAN PLACENTAL ALKALINE PHOSPHATASE - MOLECULAR WEIGHT AND SUBUNIT STRUCTURE [J].
GOTTLIEB, AJ ;
SUSSMAN, HH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1968, 160 (02) :167-&
[7]   STRUCTURAL COMPARISON OF ECTOPIC AND NORMAL PLACENTAL ALKALINE-PHOSPHATASE [J].
GREENE, PJ ;
SUSSMAN, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (10) :2936-2940
[9]   Inulin glasses for the stabilization of therapeutic proteins [J].
Hinrichs, WLJ ;
Prinsen, MG ;
Frijlink, HW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 215 (1-2) :163-174
[10]   CATALYTIC PROPERTIES OF ALKALINE-PHOSPHATASE FROM PIG KIDNEY [J].
HIWADA, K ;
WACHSMUTH, ED .
BIOCHEMICAL JOURNAL, 1974, 141 (01) :283-291