Conformational Space of the Translocation Domain of Botulinum Toxin: Atomistic Modeling and Mesoscopic Description of the Coiled-Coil Helix Bundle
DOI10.5281/zenodo.10680007Zenodo10680007MaRDI QIDQ6717619FDOQ6717619
Dataset published at Zenodo repository.
Martin Michael Müller, Grazia Cottone, Thérèse E. Malliavin
Publication date: 19 February 2024
Copyright license: Creative Commons Attribution 4.0 International
The toxicity of botulinum multi-domain neurotoxins (BoNTs) arises from a sequence of molecular events, in which the translocation of the catalytic domain through the membrane of a neurotransmitter vesicle plays a key role. A structural study (Lam et al., Nat. Comm., 2018) of the translocation domain of BoNTs suggests that the interaction with the membrane is driven by the transition of an helical switch towards a hairpin. Atomistic simulations in conjunction with the mesoscopic Twister model are used to investigate the consequences of this proposition for the toxinmembrane interaction. The conformational mobilities of the domain, as well as the effect of the membrane, implicitly examined by comparing water and waterethanol solvents, lead to the conclusion that the transition of the switch modifies the internal dynamics and the effect of membrane hydrophobicity on the whole protein. The central two helices, helix 1 and helix 2, forming two coiled-coil motifs, are analyzed using the Twister model, in which the initial deformation of the membrane by the protein is caused by the presence of local torques arising from asymmetric positions of hydrophobic residues. Different torque distributions are observed depending on the switch conformations and permit an origin for the mechanism opening the membrane to be proposed.
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