MASP 2, a complement-fixing enzyme, and uses for it
View Patent ↗The invention relates to the discovery and characterization of mannan binding lectin-associated serine protease-2 (MASP-2), a new serine protease that acts in the MBLectin complement fixation pathway.
1. A method of identifying an inhibitor of MASP-2 that is capable of inhibiting MASP-2 activity comprising assessing MASP-2 activity in the presence and absence of a candidate inhibitor wherein said inhibitor of MASP-2 activity is (1) an antibody which specifically binds to MASP-2 or an antibody fragment which specifically binds to MASP-2, (2) a serine protease inhibitor, or (3) a polypeptide fragment of MASP-2, wherein assessing MASP-2 activity comprises measuring MASP-2 mediated MBLectin complement pathway activation in an in vitro assay when MASP-2 is present as part of an MBL/MASP complex.
2. The method according to claim 1 , wherein said inhibitor directly inhibits the serine protease activity of MASP-2.
3. The method according to claim 1 , wherein said inhibitor inhibits the MBL-binding activity of MASP-2 and thereby inhibits formation of a functional complex of MASP-2 and MBL.
4. The method according to claim 1 , wherein said inhibitor is an antibody which specifically binds MASP-2 or an antibody fragment which specifically binds MASP-2.
5. The method according to claim 1 , wherein the serine protease inhibitor is an organic molecule which is not of a peptide nature.
6. The method according to claim 5 , wherein the serine protease inhibitor comprises 4-(2-aminoethyl)benzenesulfenyl fluoride, phenylmethyl sulfonyl fluoride (PMSF) or benzamidine.
7. The method according to claim 1 , wherein the inhibitor is a polypeptide fragment of MASP-2.
8. The method according to claim 7 , wherein the inhibitor is the 52 kDa or 20 kDa N-terminal fragment of MASP-2 polypeptide.
9. The method according to claim 1 , wherein the MASP-2 mediated MBLectin complement pathway activation is measured under conditions which eliminate activation from the classical pathway.