11tg

NMR solution structure of Manduca sexta pro-moricin-6

spinqualitylabelsall models 11tg Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 11tg is a 1 chain structure with sequence from Manduca sexta. Full experimental information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Solution NMR, models Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Publication Abstract from PubMed Antimicrobial peptides (AMPs) are effectors of innate immunity, which directly kill invading microbes. In insects, alpha-helical AMPs such as moricins are synthesized as inactive precursors requiring proteolytic activation by dipeptidyl peptidase IVs (DPP4s). However, the biochemical basis and functional consequence of this process remain poorly understood. Here, we identify and characterize two DPP4 enzymes from Manduca sexta, DPP4A and DPP4B. Both genes were cloned and expressed in baculovirus-infected Sf9 cells. The recombinant enzymes were purified and biochemically characterized. DPP4A and DPP4B displayed distinct catalytic properties, with K(M) at 496 and 102 muM Ala-Pro-p-nitroanilide, V(max) at 30 and 91 U/mug, and optimal pH at 8.0 and 9.0, respectively. Expression profiling revealed immune inducibility in the fat body following a bacterial challenge, while DPP4B showed elevated expression in the midgut of larvae and pupae, suggesting roles in immunity, digestion, and development. To examine the functional significance of DPP4-mediated processing, we analyzed the activation of M. sexta pro-moricin-6, which has an N-terminal APEP tetrapeptide. Removal of this pro-region by DPP4A or DPP4B generated mature moricin-6 and resulted in a approximately 10-fold increase in antimicrobial activity against Bacillus megaterium, confirming sequential cleavage of two Xaa-Pro dipeptides as the activation mechanism. Structural analyses by solution NMR showed that mature moricin-6 adopts a stable, continuous alpha-helix, whereas pro-moricin-6 exhibits a localized helical distortion near the N-terminus. Molecular dynamics simulation of the peptides in a POPC membrane further demonstrated that proteolytic processing stabilizes an extended amphipathic alpha-helix optimized for antimicrobial function. Together, these results establish the biochemical and biological roles of DPP4A and DPP4B in AMP activation and reveal how limited proteolysis precisely regulates alpha-helical AMP structure and potency in insects. Dipeptidyl peptidase IV processing activates Manduca sexta pro-moricin-6: structural basis of enhanced antimicrobial activity.,Hou C, Su A, Combs P, Roy S, Marek S, Cook GA, Prakash O, Jiang H Insect Biochem Mol Biol. 2026 Apr 4;191:104553. doi: 10.1016/j.ibmb.2026.104553. PMID:41941917 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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