Development of a novel antibody probe useful for domoic acid detection

被引:32
作者
Zhou, Yu [1 ]
Zhang, Yuan-Yuan [1 ]
Shen, Qing-Feng [1 ]
Lu, Shi-Ying [1 ]
Ren, Hong-Lin [1 ]
Li, Yan-Song [1 ]
Liu, Zeng-Shan [1 ]
Pan, Feng-Guang [1 ]
Meng, Xian-Mei [1 ]
Zhang, Jun-Hui [1 ]
机构
[1] Jilin Univ, Inst Zoonosis, Minist Educ, Key Lab Zoonosis Res, Changchun 130062, Peoples R China
基金
中国国家自然科学基金;
关键词
Immunological method; Hybridoma cell line; Marine toxin; Monoclonal antibody; Domoic acid; Lymph node cell; MONOCLONAL-ANTIBODIES; PECTEN-MAXIMUS; PROTEIN; IMMUNOASSAY; GENERATION; CANCER; COAST;
D O I
10.1016/j.bios.2009.03.023
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The generation of monoclonal antibody (mAb) against marine toxins call serve as a valuable probe to detect this kind of compounds by immunological methods. However, traditional approaches to mAb generation usually need a comparative large quantity of standard substance (more than 400 mu g mouse(-1)), and a comparative long immunization period (more than 6 weeks). Here we report a simple,inexpensive and fast protocol for the generation of monoclonal antibody probe specific for domoic acid (DA). In the method, lymph node cells were harvested from the Balb/C mice of hind footpad injection and fused with murine myeloma cells SP2/0 for hybridoma generation. This method for the preparation of mAb for DA has two main advantages: (a) there is no need for large-scale expensive antigen (only 70 mu g antigen for one mouse); (b) immunization protocol can be accomplished within 16 days. Some characteristics of the mAb were studied and a direct competitive ELISA for the detection of DA using the mAb as a probe was developed. The detection limit was 0.41 ng well(-1) In phosphate buffered saline (PBS) and 0.53 ng well(-1) in blue mussel Mytilus edulis. The recoveries of DA from mussel and PBS buffer were from 94.8% to 105.1% and from 96.2% to 103.7%, respectively. Thus, the newly developed direct competitive ELISA using the mAb appears to be a reliable and useful method for monitoring of DA in shellfish (228 words). (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3159 / 3163
页数:5
相关论文
共 27 条
[1]
Monoclonal antibody therapy of cancer [J].
Adams, GP ;
Weiner, LM .
NATURE BIOTECHNOLOGY, 2005, 23 (09) :1147-1157
[2]
Sea bird mortality at Cabo San Lucas, Mexico: Evidence that toxic diatom blooms are spreading [J].
Beltran, AS ;
PalafoxUribe, M ;
GrajalesMontiel, J ;
CruzVillacorta, A ;
Ochoa, JL .
TOXICON, 1997, 35 (03) :447-453
[3]
Spatial variability of domoic acid concentration in king scallops Pecten maximus off the southeast coast of Ireland [J].
Bogan, Y. M. ;
Bender, K. ;
Hervas, A. ;
Kennedy, D. J. ;
Slater, J. W. ;
Hess, P. .
HARMFUL ALGAE, 2007, 6 (01) :1-14
[4]
Campbell DA, 2001, J SHELLFISH RES, V20, P75
[5]
Comparison of hybridoma screening methods for the efficient detection of high-affinity hapten-specific monoclonal antibodies [J].
Cervino, Christian ;
Weber, Ekkehard ;
Knopp, Dietmar ;
Niessner, Reinhard .
JOURNAL OF IMMUNOLOGICAL METHODS, 2008, 329 (1-2) :184-193
[6]
Development and characterization of monoclonal antibodies to spring viraemia of carp virus [J].
Chen, Zhong-Yuan ;
Liu, Hong ;
Li, Zheng-Qiu ;
Zhang, Qi-Ya .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2008, 123 (3-4) :266-276
[7]
Production of monoclonal antibodies that recognize the extracellular domain of mouse Langerin/CD207 [J].
Cheong, Cheolho ;
Idoyaga, Juliana ;
Do, Yoonkyung ;
Pack, Maggi ;
Park, Sung Ho ;
Lee, Haekyung ;
Kang, Young-Sun ;
Choi, Jae-Hoon ;
Kim, Jae Y. ;
Bonito, Anthony ;
Inaba, Kayo ;
Yamazaki, Sayuri ;
Steinman, Ralph M. ;
Park, Chae Gyu .
JOURNAL OF IMMUNOLOGICAL METHODS, 2007, 324 (1-2) :48-62
[8]
Accumulation, transformation and tissue distribution of domoic acid, the amnesic shellfish poisoning toxin, in the common cuttlefish, Sepia officinalis [J].
Costa, PR ;
Rosab, R ;
Duarte-Silva, A ;
Brotas, V ;
Sampayo, MAM .
AQUATIC TOXICOLOGY, 2005, 74 (01) :82-91
[9]
A simple hybridoma screening method for high-affinity monoclonal antibodies using the signal ratio obtained from time-resolved fluorescence assay [J].
Daigo, K ;
Sugita, S ;
Mochizuki, Y ;
Iwanari, H ;
Hiraishi, K ;
Miyano, K ;
Kodama, T ;
Hamakubo, T .
ANALYTICAL BIOCHEMISTRY, 2006, 351 (02) :219-228
[10]
DONG ZW, 2002, ANTIBODY ENG, P281