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中国生物工程杂志

China Biotechnology
China Biotechnology  2018, Vol. 38 Issue (12): 65-75    DOI: 10.13523/j.cb.20181209
Orginal Article     
Progress in the Synthesis of Artificial Antigen
LI Rong-qing,QUAN Chun-shan(),ZHANG Li-ying(),LIU Jia-lu,ZHANG Xiang,SHANG Fei
Key Laboratory of the State Ethnic Affairs Commission-Ministry of Education,School of Life Science,Dalian Nationalities University,Dalian 116600,China
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Abstract  

The immunoassay with small molecular as a hapten has been used in many fields, such as food and drug, environmental protection and so on. It has obtained more ideal detection results. The small molecular must be coupled with the carrier to form an artificial antigen, which can indirectly induce the proliferation and differentiation of B cells by using the epitopes of T cells, and then produce specific antibodies. The synthesis of high efficient artificial antigen is the precondition and key to ensure immune analysis. Based on this, the design and synthesis methods, the selection of the carrier, the coupling method of the hapten and the carrier, the purification and identification methods of the artificial antigen, both here and abroad are reviewed.



Key wordsHapten      Artificial antigen      Selection of carrier      Purification of antigen      Identification of antigen     
Received: 25 June 2018      Published: 10 January 2019
ZTFLH:  Q816  
Corresponding Authors: Chun-shan QUAN,Li-ying ZHANG     E-mail: mikyeken@dlnu.edu.cn;zhangly@dlnu.edu.cn
Cite this article:

LI Rong-qing,QUAN Chun-shan,ZHANG Li-ying,LIU Jia-lu,ZHANG Xiang,SHANG Fei. Progress in the Synthesis of Artificial Antigen. China Biotechnology, 2018, 38(12): 65-75.

URL:

https://manu60.magtech.com.cn/biotech/10.13523/j.cb.20181209     OR     https://manu60.magtech.com.cn/biotech/Y2018/V38/I12/65

Fig.1 Phosphohistidine structural analogues used as hapten
Antiserum dilutionCoating antigen hapten (ng/well)IC50 (ng/ml)
1∶10 00010 000
1∶10 0002 840
 
Fig.2 Stilbestrol hapten
Fig.3 Effect of the linking spacer length on the coupling ratio of artificial antigen
Fig.4 Norepinephrine hapten(a) and 3-amino-2-oxazolidinone hapten (b)
 
Fig.5 Synthetic route of hapten TBBPA-D2
活性基团偶联方法反应原理实例
-OH高碘酸钠反应法[32]
氰脲酰氯反应法
[33]
N,N-二琥珀酰亚胺基
碳酸酯反应法
[34]
N,N-羰基二咪唑反应法[35]
活性基团偶联方法反应原理实例
Linker法[35]
多酸酐反应法[36]
卤代硝基苯反应法[37]
-COOH偶氮苯甲酸法[38]
碳二亚胺反应法[39]
混合酸酐反应法[40]
N,N-羰基二咪唑反应法[41]
活泼酯反应法[42]
-NH2戊二醛反应法[5]
活性基团偶联方法反应原理实例
碳二亚胺反应法[43]
异氰酸反应法[44]
N-羟基琥珀酰亚胺酯反应法[45]
重氮化反应法[20]
对肼基苯甲酸反应法[46]
肟化反应法[47]
曼尼希反应法[48]
-SH马来酰亚胺基反应法[49]
双马来酰亚胺基反应法[50]
-COOCH3叠氮化反应法[51]
 
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