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TitleA molecular basis for stoichiometric enzyme encapsulation in the vitamin B2 biosynthesis compartment.
Journal, issue, pagesNat Commun, Year 2026
Publish dateMay 16, 2026
AuthorsLukasz Koziej / Jedrzej Pankowski / Monika Stefanska / Daniel Jankowski / Agnieszka Gawin / V Vishal Malolan / Juha T Huiskonen / Takahiro Kosugi / Yusuke Azuma /
PubMed AbstractEncapsulating metabolic enzymes within protein cages enhances catalytic efficiency through substrate channeling. The vitamin B2 biosynthesis system, in which a dodecahedral lumazine synthase (LS) ...Encapsulating metabolic enzymes within protein cages enhances catalytic efficiency through substrate channeling. The vitamin B2 biosynthesis system, in which a dodecahedral lumazine synthase (LS) cage encapsulates a homotrimeric riboflavin synthase (RS), exemplifies this strategy, yet the molecular basis for this stoichiometric enzyme encapsulation has remained elusive. Here, cryogenic electron microscopy structures reveal a hierarchical assembly mechanism that ensures the defined host-guest ratio. RS C-terminal cage-localization signal peptides anchor at LS pentamer-pentamer interfaces early during assembly, stabilizing open intermediates that, together with delayed later-stage cage closure, extend the loading window until guest incorporation is complete. RS spatial occupancy avoids overloading, while a molecular lock upon final closure prevents disassembly. The elucidated anchoring mechanism enabled structure-based phylogenetic analysis across diverse organisms, suggesting multiple independent evolutionary origins of this modular encapsulation strategy. This naturally occurring architecture provides design principles for engineering synthetic catalytic compartments with programmable stoichiometric control.
External linksNat Commun / PubMed:42143052
MethodsEM (single particle)
Resolution1.71 - 2.78 Å
Structure data

EMDB-54381, PDB-9ryi:
Aquifex aeolicus lumazine synthase 12-pentamer cage in complex with I-symmetry-masked riboflavin synthase
Method: EM (single particle) / Resolution: 1.71 Å

EMDB-54382, PDB-9ryj:
Aquifex aeolicus lumazine synthase 11-pentamer cage in complex with C5-symmetrized riboflavin synthase C-termini
Method: EM (single particle) / Resolution: 1.99 Å

EMDB-54383, PDB-9ryk:
Aquifex aeolicus lumazine synthase 11-pentamer cage in complex with riboflavin synthase trimer
Method: EM (single particle) / Resolution: 2.6 Å

EMDB-54385, PDB-9rym:
Aquifex aeolicus lumazine synthase 10-pentamer cage in complex with riboflavin synthase trimer
Method: EM (single particle) / Resolution: 2.78 Å

EMDB-54386, PDB-9ryn:
Aquifex aeolicus lumazine synthase 12-pentamer cage
Method: EM (single particle) / Resolution: 1.71 Å

EMDB-54387, PDB-9ryo:
Aquifex aeolicus lumazine synthase 11-pentamer cage
Method: EM (single particle) / Resolution: 2.09 Å

EMDB-54388, PDB-9ryp:
Aquifex aeolicus lumazine synthase R29A mutant 12-pentamer cage
Method: EM (single particle) / Resolution: 1.71 Å

EMDB-54389, PDB-9ryq:
Aquifex aeolicus lumazine synthase R29A mutant 11-pentamer cage
Method: EM (single particle) / Resolution: 2.08 Å

EMDB-54392, PDB-9ryu:
Aquifex aeolicus lumazine synthase L121A mutant 12-pentamer cage
Method: EM (single particle) / Resolution: 1.71 Å

EMDB-54393, PDB-9ryv:
Aquifex aeolicus lumazine synthase L121A mutant 11-pentamer cage
Method: EM (single particle) / Resolution: 2.49 Å

EMDB-54394, PDB-9ryw:
Aquifex aeolicus lumazine synthase I125A mutant 12-pentamer cage
Method: EM (single particle) / Resolution: 1.71 Å

EMDB-54395, PDB-9ryx:
Aquifex aeolicus lumazine synthase I125A mutant 11-pentamer cage
Method: EM (single particle) / Resolution: 2.31 Å

Chemicals

ChemComp-PO4:
PHOSPHATE ION

ChemComp-HOH:
WATER

Source
  • aquifex aeolicus vf5 (bacteria)
KeywordsBIOSYNTHETIC PROTEIN / protein cage / protein engineering / self-assembly / geometry / pentamer / encapsulation

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