Poly-N-hydroxyethylacrylamide as a novel, adsorbed coating for protein separation by capillary electrophoresis

被引:87
作者
Albarghouthi, MN
Stein, TM
Barron, AE
机构
[1] Northwestern Univ, Dept Chem Engn, Evanston, IL 60208 USA
[2] Walkersville Inc, Cambrex Bio Sci, Walkersville, MD USA
关键词
capillary coating; capillary electrophoresis; dynamic coating; poly-N-hydroxyethylacrylamide; protein separation;
D O I
10.1002/elps.200390150
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present the polymer poly-N-hydroxyethylacrylamide (PHEA) (trade name, polyDuramide(TM)) as a novel, hydrophilic, adsorbed capillary coating for electrophoretic protein analysis. Preparation of the PHEA coating requires a simple and fast (30 min) protocol that can be easily automated in capillary electrophoresis instruments. Over the pH range of 3-8.4, the PHEA coating is shown to reduce electroosmotic flow (EOF) by about 2 orders of magnitude compared to the bare silica capillary. In a systematic comparative study, the adsorbed PHEA coating exhibited minimal interactions with both acidic and basic proteins, providing efficient protein separations with excellent reproducibility on par with a covalent polyacrylamide coating. Hydrophobic interactions between proteins and a relatively hydrophobic poly-N,N-dimethylacrylamide (PDMA) adsorbed coating, on the other hand, adversely affected separation reproducibility and efficiency. Under both acidic and basic buffer conditions, the adsorbed PHEA coating produced an EOF suppression performance comparable to that of covalent polyacrylamide coating and superior to that of adsorbed PDMA coating. The protein separation performance in PHEA-coated capillaries was retained for 275 consecutive protein separation runs at pH 8.4, and for more than 800 runs at pH 4.4. The unique and novel combination of hydrophilicity and adsorptive coating ability of PHEA makes it a suitable wall coating for automated microscale analysis of proteins by capillary array systems.
引用
收藏
页码:1166 / 1175
页数:10
相关论文
共 58 条
  • [1] Albarghouthi MN, 2002, ELECTROPHORESIS, V23, P1429, DOI 10.1002/1522-2683(200205)23:10<1429::AID-ELPS1429>3.0.CO
  • [2] 2-A
  • [3] Separation of proteins by capillary electrophoresis using an epoxy based hydrophilic coating
    Bao, JJ
    [J]. JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2000, 23 (01) : 61 - 78
  • [4] Belen'kii BG, 1998, J ANAL CHEM+, V53, P940
  • [5] Protein sizing on a microchip
    Bousse, L
    Mouradian, S
    Minalla, A
    Yee, H
    Williams, K
    Dubrow, R
    [J]. ANALYTICAL CHEMISTRY, 2001, 73 (06) : 1207 - 1212
  • [6] CELLULOSE ACETATE-COATED FUSED-SILICA CAPILLARIES FOR THE SEPARATION OF PROTEINS BY CAPILLARY ZONE ELECTROPHORESIS
    BUSCH, MHA
    KRAAK, JC
    POPPE, H
    [J]. JOURNAL OF CHROMATOGRAPHY A, 1995, 695 (02) : 287 - 296
  • [7] Chiari M, 2000, ELECTROPHORESIS, V21, P909, DOI 10.1002/(SICI)1522-2683(20000301)21:5<909::AID-ELPS909>3.0.CO
  • [8] 2-L
  • [9] Synthesis and characterization of capillary columns coated with glycoside bearing polymer
    Chiari, M
    DellOrto, N
    Gelain, A
    [J]. ANALYTICAL CHEMISTRY, 1996, 68 (17) : 2731 - 2736
  • [10] CAPILLARY ELECTROPHORETIC SEPARATION OF PROTEINS USING STABLE, HYDROPHILIC POLY(ACRYLOYLAMINOETHOXYETHANOL)-COATED COLUMNS
    CHIARI, M
    NESI, M
    SANDOVAL, JE
    PESEK, JJ
    [J]. JOURNAL OF CHROMATOGRAPHY A, 1995, 717 (1-2) : 1 - 13