Detection method of human myelin oligodendroglia glycoprotein self immune antibody
A technology for autoimmune antibodies and detection methods, applied in the field of detection of human myelin oligodendrocyte glycoprotein autoimmune antibodies, can solve the problems of inability to specifically bind antibodies, specificity and sensitivity, etc. problems, achieve important research and practical value, good specificity, and high detection efficiency
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2017-10-20
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Abstract
Description
technical field
[0001] The invention relates to the field of biological detection, in particular to a detection method of human myelin oligodendrocyte glycoprotein autoimmune antibody. Background technique
[0002] Myelin oligodendrocyte glycoprotein (MOG) is a myelin protein component that is specifically produced by oligodendrocytes and exists in the outermost layer of myelin in the central nervous system (CNS). The physiological functions of MOG include the constituent proteins of myelin, cell surface adhesion molecules mediating the interaction between myelin and extracellular matrix, regulating the stability of microtubules and participating in the activation of the complement system, etc. Studies at home and abroad have shown that autoimmune antibodies against MOG can be detected in a variety of central nervous system inflammatory demyelinating diseases, such as multiple sclerosis (MS), acute myelitis (AM) and neuromyelitis optica (NMO). . And MOG antibody-positive p...
Examples
Embodiment
[0019] 1 Construction of expression vector
[0020] Try a variety of MOG expression vectors, including pcDNA3.1-MOG, pcDNA3.1-MOG-GFP (expressing MOG and GFP fusion protein), pEGFP-IRES-MOG, etc., by screening and comparing the level of MOG antigen expressed on the cell surface, the expression vector pEGFP-IRES-MOG(expression vector2)( figure 1 ) MOG antigen expressed on the cell surface was significantly higher than other expression vectors.
[0021] The pEGFP-IRES-MOG vector was constructed by inserting the internal ribosome entry site sequence (IRES) downstream of the green fluorescent protein (GFP) gene in the eukaryotic expression vector pEGFP vector (with CMV promoter), and cloning after the IRES The cDNA sequence encoding the full-length human MOG was obtained. The human calnexin gene was cloned into the pcDNA3.1 vector to obtain the pcDNA-clanexin expression vector.
[0022] 2 chaperone calnexin promotes membrane expression of MOG antigen
[0023] MOG autoimmune an...