Serine protease homolog pairs CLIPA4-A6, A4-A7Δ, and A4-A12 act as cofactors for proteolytic activation of prophenoloxidase-2 and -7 in Anopheles gambiae.

Phenoloxidase (PO) catalyzed melanization and other insect immune responses are mediated by serine proteases (SPs) and their noncatalytic homologs (SPHs). Many of these SP-like proteins have a regulatory clip domain and are called CLIPs. In most insects studied so far, PO precursors are activated by a PAP (i.e., PPO activating protease) and its cofactor of clip-domain SPHs. Although melanotic encapsulation is a well-known refractory mechanism of mosquitoes against malaria parasites, it is unclear if a cofactor is required for PPO activation. In Anopheles gambiae , CLIPA4 is 1:1 orthologous to Manduca sexta SPH2; CLIPs A5−7, A12–14, A26, A31, A32, E6, and E7 are 11:4 orthologous to M. sexta SPH1a, 1b, 4, and 101, SPH2 partners in the cofactors. Here we produced proCLIPs A4, A6, A7Δ, A12, and activated them with CLIPB9 or M. sexta PAP3. A. gambiae PPO2 and PPO7 were expressed in Escherichia coli for use as PAP substrates. CLIPB9 was mutated to CLIPB9 Xa by including a Factor X a cleavage site. CLIPA7Δ was a deletion mutant with a low complexity region removed. After PAP3 or CLIPB9 Xa processing, CLIPA4 formed a high M r complex with CLIPA6, A7Δ or A12, which assisted PPO2 and PPO7 activation. High levels of specific PO activity (55−85 U/μg for PO2 and 1131−1630 U/μg for PO7) were detected in vitro , indicating that cofactor-assisted PPO activation also occurs in this species. The cleavage sites and mechanisms for complex formation and cofactor function are like those reported in M. sexta and Drosophila melanogaster. In conclusion, these data suggest that the three (and perhaps more) SPHI-II pairs may form cofactors for CLIPB9-mediated activation of PPOs for melanotic encapsulation in A. gambiae. [Display omitted] • A. gambiae CLIPB9x a cleaved proCLIPA4, 6, 7Δ, and 12 to form its own cofactors. • M. sexta PAP3 more efficiently produced the cofactors for A. gambiae PPO activation. • CLIPs A6, A7Δ, or A12 pairs with CLIPA4 for PPO2/7 activation by CLIPB9 or PAP3. • Cleavages of pro-cSPHIs at site-1 and -2 and pro-cSPHII at site-1 are conserved. • Direct biochemical analysis based on orthology is useful for functional elucidation. [ABSTRACT FROM AUTHOR]