作者: Wilhelm J. Schwaeble , Cordula M. Stover , Steffen Thiel , Nicholas J. Lynch
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摘要: Recently, we described two novel constituents of the multimolecular initiation complex mannan-binding lectin (MBL) pathway complement activation, a serine protease 76 kDa, termed MASP-2, and MASP-2 related plasma protein 19 MAp19. Upon activation MBL/MASPs/MAp19 complex, cleaves fourth component C4, while role MAp19 within MBL/MASP-1/MASP-2/MAp19 remains to be clarified. In humans, mRNA species encoding (2.6 kb) (1.0 arise by an alternative polyadenylation/splicing mechanism from single structural gene. Here, report complete primary structures rat homologue mouse We show that both are part MBL demonstrate their exclusively hepatic biosynthesis. Southern blot PCR analyses genomic DNA indicate as in encoded