11TJ

NMR solution structure of Manduca sexta moricin-6

Summary for 11TJ

• Entry DOI: 10.2210/pdb11tj/pdb
• NMR Information: BMRB: 31296
• Descriptor: Moricin-6 (1 entity in total)
• Functional Keywords: antimicrobial peptide, amp, insect immunity, proteolytic activation, s8 serine protease, dpp4, molecular dynamics simulation, antimicrobial protein
• Biological source: Manduca sexta (tobacco hornworm)
• Total number of polymer chains: 1
• Total formula weight: 4026.76

Authors

Hou, C.,Su, A.,Combs, P.,Roy, S.,Marek, S.,Cook, G.A.,Prakash, O.,Jiang, H. (deposition date: 2026-03-12, release date: 2026-04-22)

Primary citation

Hou, C.,Su, A.,Combs, P.,Roy, S.,Marek, S.,Cook, G.A.,Prakash, O.,Jiang, H.
Dipeptidyl peptidase IV processing activates Manduca sexta pro-moricin-6: structural basis of enhanced antimicrobial activity.
Insect Biochem.Mol.Biol., 191:104553-104553, 2026

PubMed Abstract: Antimicrobial peptides (AMPs) are effectors of innate immunity, which directly kill invading microbes. In insects, α-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 at 496 and 102 μM Ala-Pro-p-nitroanilide, V at 30 and 91 U/μg, 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 ∼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 α-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 α-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 α-helical AMP structure and potency in insects.

PubMed: 41941917
DOI: 10.1016/j.ibmb.2026.104553

Experimental method

SOLUTION NMR