Lambris J D, Alsenz J, Schulz T F, Dierich M P
Biochem J. 1984 Jan 1;217(1):323-6. doi: 10.1042/bj2170323.
The properdin-binding site in the human third complement component (C3) was mapped by using isolated C3b, C3c, alpha- and beta-chains of C3 and C3 polypeptide fragments and an enzyme-linked-immunosorbent-assay procedure. The C3 chains and the polypeptide fragments were purified to homogeneity by preparative sodium dodecyl sulphate/polyacrylamide-gel electrophoresis. The alpha-chain polypeptides included a 68 kDa and a 43 kDa polypeptide, which were generated by cleavage of C3b with factors I and H, and a 40 kDa, 33 kDa (C3d) and 27 kDa polypeptide, which were generated by cleavage of C3b with porcine elastase. It was shown that properdin binds to C3b, C3c, alpha-chain, and to the 43 kDa (factor-I + H-derived), as well as to 40 kDa (elastase-derived) alpha-chain fragment, but not to the beta-chain 68 kDa, 33 kDa (C3d) and 27 kDa alpha-chain fragments. Thus the binding site for properdin resides on the 40-43 kDa C-terminal alpha-chain fragment of C3.
通过使用分离的C3b、C3c、C3的α链和β链、C3多肽片段以及酶联免疫吸附测定法,绘制了人第三补体成分(C3)中的备解素结合位点。通过制备性十二烷基硫酸钠/聚丙烯酰胺凝胶电泳将C3链和多肽片段纯化至同质。α链多肽包括由因子I和H切割C3b产生的68 kDa和43 kDa多肽,以及由猪弹性蛋白酶切割C3b产生的40 kDa、33 kDa(C3d)和27 kDa多肽。结果表明,备解素与C3b、C3c、α链、43 kDa(因子I+H衍生)以及40 kDa(弹性蛋白酶衍生)α链片段结合,但不与β链、68 kDa、33 kDa(C3d)和27 kDaα链片段结合。因此,备解素的结合位点位于C3的40-43 kDa C末端α链片段上。