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Enzyme amplification as detection tool in continuous-flow systems II. On-line coupling of liquid chromatography to enzyme-amplified biochemical detection after pre-column derivatization with biotin
被引:5
|作者:
van Bommel, MR
de Jong, APJM
Tjaden, UR
Irth, H
van der Greef, J
机构:
[1] Leiden Univ, Leiden Amsterdam Ctr Drug Res, Div Analyt Chem, NL-2300 RA Leiden, Netherlands
[2] Dutch Inst Publ Hlth & Environm, Div Mol Spectrometry, NL-3720 BA Bilthoven, Netherlands
关键词:
enzyme amplification;
derivatization;
LC;
detection;
biotin;
alkaline phosphatase;
D O I:
10.1016/S0021-9673(99)00745-1
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Enzyme-amplified biochemical detection (EA-BCD) was used as a post-column detection technique, coupled on-line with high-performance liquid chromatography (HPLC). The enzyme detection system was developed to detect biotin or biotin containing compounds. Biotinylation is widely used to label analytes of interest ranging from small molecules to proteins and DNA. Naphthalene aldehyde and anthracene aldehyde were used as model compounds. Both compounds were biotinylated off-line with biotin aminocaproic hydrazide (BACH), On-column biotinylation was performed by preconcentration of anthracene aldehyde on copper phthalocyanine. After biotinylation, samples were introduced to the HPLC system. Enzyme-labeled streptavidin, which possesses high affinity to biotin, was added post-column to the HPLC effluent. Excess of enzyme-labeled affinity protein was removed by means of an immobilized biotin column. After separation of free and bound fraction, substrate was added, which was converted to a fluorescent product by the enzyme label. Using alkaline phosphatase as an enzyme label, a mass detection limit after on-column preconcentration and biotinylation of 250 fmol was achieved. (C) 1999 Elsevier Science B.V. All rights reserved.
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页码:397 / 409
页数:13
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