TITLE:
Production and Characterization of Recombinant Rat Non-Collagen Domain of α3 Chain of Type IV Collagen α3 (IV) NC1 Antigen
AUTHORS:
Afsana Munni
KEYWORDS:
Auto-Immuno Kidney Disease, Glomerulonephritis Disease, Glomerular Basement Membrane, α3 (IV) NC1-Non-Collagen Domain of α3 Chain of Type IV Collagen α3 (IV), Antibody(Ab), Antigen (Ag), Anti Glomerular Basement Membrane, Experimental Autoimmune Glomerulonephritis, Enzyme-Linked Immunosorbent Assay (ELISA), Human Embryonic Kidney (HEK), Ig-Immunoglobulin (IgG, IgA), IgAN-IgA nephropathy
JOURNAL NAME:
CellBio,
Vol.5 No.3,
August
23,
2016
ABSTRACT: The glomerulonephritis disease is characterized by inflammation of glomeruli or small blood vessels in the kidney that causes kidney diseases. The reason of glomerulonephritis disease is to deposit the anti-GBM auto antibody in the glomerular basement membrane. The type IV collagen is the main component of glomerular basement membrane that has α3 chain of type (IV) collagen of non-collagenous domain which contains N-terminal 7S domain, a triple helical collagenous domain and C-terminal non-collagenous glomerular domain (NC1). The amino terminal of α3 (IV) NC1 that induces the Experimental Autoimmuno Glomerulonephritis (EAG) in rat model has been identified. The recombinant rat α3 (IV) NC1 antigen has nine amino acid spans that are consistent with antibody or T cell epitope that induces in EAG. The research is carried out on the recombinant rat α3 (IV) NC1 production, purification, quantification, and characterization. The circulation of anti-GBM antibody in glomerular basement membrane can be measured by the ELISA assay. In addition, the recombinant rat antigen is secreted in HEK293 cell supernatant that is purified by Anti-FLAG M2 monoclonal IgG antibody affinity column and characterized and quantified by SDS-PAGE gel electrophoresis and Western blotting techniques.