A cyclic peptide-polymer probe for the detection of Clostridium botulinum neurotoxin serotype A

被引:23
作者
Ma, Hongzheng
Zhou, Bin
Kim, YoungSoo
Janda, Kim D.
机构
[1] Scripps Res Inst, Worm Inst Res & Med, Dept Chem, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Worm Inst Res & Med, Dept Immunol, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
关键词
cyclic peptide; polymer; phage display; Botulinum neurotoxin; ELISA;
D O I
10.1016/j.toxicon.2006.03.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A Botulinum neurotoxin serotype A (BoNT/A) ELISA detection system was developed based upon an 11-mer cyclic peptide, termed C11-019, that was identified through peptide phage display technology. The assay employs a sandwich format using the C11-019 cyclic peptide attached to a PEMA (poly(ethylene maleic anhydride)) matrix as the capture phase and anti-BoNT/A polyclonal antibodies as the detection phase. Results reported demonstrate that the C11-019 peptide-polymer can specifically bind to BoNT/A with no cross-reactivity to other serotypes examined in assay buffers and a variety of body fluids and foodstuffs. When a highly sensitive chemiluminescent substrate was engaged, the detection of 1 pg/mL could be readily achieved within 3 h with a linear range of 0.1-1 ng/mL. These results demonstrate that an inexpensive peptide-polymer-based capture ELISA system can be used for rapid, sensitive and highly specific BoNT detection. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:901 / 908
页数:8
相关论文
共 17 条
[1]  
Amon S. S., 2001, JAMA-J AM MED ASSOC, V285, P1059
[2]   SENSITIVE ENZYME-LINKED-IMMUNOSORBENT-ASSAY FOR DETECTION OF CLOSTRIDIUM-BOTULINUM NEUROTOXIN-A, NEUROTOXIN-B, AND NEUROTOXIN-E USING SIGNAL AMPLIFICATION VIA ENZYME-LINKED COAGULATION ASSAY [J].
DOELLGAST, GJ ;
TRISCOTT, MX ;
BEARD, GA ;
BOTTOMS, JD ;
CHENG, T ;
ROH, BH ;
ROMAN, MG ;
HALL, PA ;
BROWN, JE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (09) :2402-2409
[3]  
GAMEZ F, 2004, 104 GEN M AM SOC MIC, P23
[4]   Influencing receptor-ligand binding mechanisms with multivalent ligand architecture [J].
Gestwicki, JE ;
Cairo, CW ;
Strong, LE ;
Oetjen, KA ;
Kiessling, LL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (50) :14922-14933
[5]   How botulinum and tetanus neurotoxins block neurotransmitter release [J].
Humeau, Y ;
Doussau, F ;
Grant, NJ ;
Poulain, B .
BIOCHIMIE, 2000, 82 (05) :427-446
[6]  
KAUTTER DA, 1984, FDA BACTERIOLOGICAL
[7]   A contiguous stretch of methionine residues mediates the energy-dependent internalization mechanism of a cell-penetrating peptide [J].
Kim, Youngsoo ;
Lillo, Antonietta ;
Moss, Jason A. ;
Janda, Kim D. .
MOLECULAR PHARMACEUTICS, 2005, 2 (06) :528-535
[8]   Sequence homology and structural analysis of the clostridial neurotoxins [J].
Lacy, DB ;
Stevens, RC .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 291 (05) :1091-1104
[9]  
Mammen M, 1998, ANGEW CHEM INT EDIT, V37, P2755
[10]   Designing a polyvalent inhibitor of anthrax toxin [J].
Mourez, M ;
Kane, RS ;
Mogridge, J ;
Metallo, S ;
Deschatelets, P ;
Sellman, BR ;
Whitesides, GM ;
Collier, RJ .
NATURE BIOTECHNOLOGY, 2001, 19 (10) :958-961