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AN INFLUENZA HEMAGGLUTININ A PEPTIDE ASSAY BASED ON THE ENZYME-MULTIPLIED IMMUNOASSAY TECHNIQUE
被引:4
|作者:
Chiu, May L.
[1
]
Lai, Denton
[1
]
Monbouquette, Harold G.
[1
]
机构:
[1] Univ Calif Los Angeles, Chem & Biomol Engn Dept, Los Angeles, CA 90095 USA
来源:
基金:
美国国家卫生研究院;
关键词:
EMIT;
enzyme multiplied immunoassay technique;
hemagglutinin A;
peptide detection;
GLUCOSE 6-PHOSPHATE DEHYDROGENASE;
BETA-GALACTOSIDASE;
LEUCONOSTOC-MESENTEROIDES;
HOMOGENEOUS IMMUNOASSAYS;
PROTEIN;
SENSITIVITY;
OPIATES;
EMIT;
D O I:
10.1080/15321819.2011.538623
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
A practical approach for constructing enzyme-multiplied immunoassay technique (EMIT)-based protein/ peptide assays is described. Normally used in small-molecule drug testing, EMIT is a homogeneous assay method that is attractive for its simplicity, sensitivity, and rapidity. The EMIT-based peptide/ protein assay was developed by conjugating a cysteine-modified HA peptide (from influenza hemagglutinin A) to the reporter enzyme, glucose-6-phosphate dehydrogenase. The 13-min assay gave a free HA limit of detection of 10 nM and proved effective for detection of a high-molecular-weight model protein tagged with HA. Similar EMIT-based assay approaches may be developed for applications in biotoxin and infectious disease detection.
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页码:1 / 17
页数:17
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