Plastic enzyme-linked immunosorbent assays (ELISA)-on-a-chip biosensor for botulinum neurotoxin A

被引:48
作者
Han, Seung-Mok
Cho, Joung-Hwan
Cho, Il-Hoon
Paek, Eui-Hwan
Oh, Hee-Bok
Kim, Bong-Su
Ryu, Chunsun
Lee, Kyunghee
Kim, Young-Kee
Paek, Se-Hwan
机构
[1] Korea Univ, Program Biomicrosyst Technol, Sungbuk Ku, Seoul 136701, South Korea
[2] Korea Univ, Technol Incubat Ctr, BioDigit Labs Corp, Sungbuk Ku, Seoul 136701, South Korea
[3] NIH, Div High Risk Pathogen Res, Ctr Infect Dis Res, Eunpyeong Ku, Seoul 122701, South Korea
[4] Korea Univ, Dept Biotechnol, Jochiwon 339800, Choongnam, South Korea
[5] Hankyong Natl Univ, Dept Chem Engn, Ansung 456749, Kyonggi, South Korea
关键词
cross-flow immuno-chromatography; enzyme label; injection-molded plastic chip; colorimetric detector; bio-defense; CROSS-FLOW CHROMATOGRAPHY; SENSITIVE DETECTION; ANTIBODIES; PURIFICATION; AFFINITY;
D O I
10.1016/j.aca.2007.01.028
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A plastic ELISA-on-a-chip (EOC) employing the concept of cross-flow immuno-chromatographic analysis was applied to the measurement of botulinum neurotoxin A (BoNT/A) as agent for bio-terrorism. Two monoclonal antibodies specific to the heavy chain of the toxin were raised and identified to form sandwich binding complexes as the pair with the analyte. For the construction of an immuno-strip, one was utilized as the capture antibody immobilized onto nitrocellulose membrane and the other as the detection coupled to an enzyme, horseradish peroxidase. The two plates of EOC used in this study were fabricated by injection molding of polycarbonate to improve the reproducibility of manufacture and, after inclusion of the immuno-strip, bonded using a UV-sensitive adhesive. Under optimal conditions of analysis, the chip produced a color signal in proportion to the analyte dose and the signal was quantified using a detector equipped with a digital camera. From the dose-response curve, the detection limit of BoNT/A was 2.0 ng mL(-1), approximately five times more sensitive than a commercial-version detection kit employing colloidal gold tracer. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 28 条
  • [1] ALBERT RM, 1993, PAWLEY IMMUNOCYTOCHE, P151
  • [2] ANNE HP, 2002, J IMMUNOL METHODS, V263, P35
  • [3] ASHRAF AS, 2003, BIOCHEMISTRY-US, V42, P12539
  • [4] BERS G, 1985, Biotechniques, V3, P276
  • [5] BLACKSHEAR PJ, 1984, METHOD ENZYMOL, V104, P237
  • [6] Expression and purification of catalytically active, non-toxic endopeptidase derivatives of Clostridium botulinum toxin type A
    Chaddock, JA
    Herbert, MH
    Ling, RJ
    Alexander, FCG
    Fooks, SJ
    Revell, DF
    Quinn, CP
    Shone, CC
    Foster, KA
    [J]. PROTEIN EXPRESSION AND PURIFICATION, 2002, 25 (02) : 219 - 228
  • [7] Colloidal gold-based immunochromatogrphic assay for detection of botulinum neurotoxin type B
    Chiao, DJ
    Shyu, RH
    Hu, CS
    Chiang, HY
    Tang, SS
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 809 (01): : 37 - 41
  • [8] Plastic ELISA-on-a-chip based on sequential cross-flow chromatography
    Cho, JH
    Han, SM
    Paek, EH
    Cho, IH
    Paek, SH
    [J]. ANALYTICAL CHEMISTRY, 2006, 78 (03) : 793 - 800
  • [9] An enzyme immunoanalytical system based on sequential cross-flow chromatography
    Cho, JH
    Paek, EH
    Cho, IH
    Paek, SH
    [J]. ANALYTICAL CHEMISTRY, 2005, 77 (13) : 4091 - 4097
  • [10] Dykman LA, 1998, COLLOID J+, V60, P700