[摘要]：Botulinum neurotoxins (BoNTs) are the most toxic proteins known The mechanism for entry into neuronal cells for serotypes A B E F and G involves a well understood dual receptor (protein and ganglioside) process however the mechanism of entry for serotypes C and D remains unclear To provide structural insights into how BoNT/D enters neuronal cells the crystal structure of the receptor binding domain (S863-E1276) for this serotype (BoNT/D-HCR) was determined at 1 65 angstrom resolution While BoNT/D-HCR adopts an overall fold similar to that observed in other known BoNT HCRs several major structural differences are present These structural differences are located at or near putative receptor binding sites and may be responsible for BoNT/D host preferences Two loops S1195-I1204 and K1236-N1244 located on both sides of the putative protein receptor binding pocket are displaced >10 angstrom relative to the corresponding residues in the crystal structures of BoNT/B and G Obvious clashes were observed in the putative protein receptor binding site when the BoNT/B protein receptor synaptotagmin II was modeled into the BoNT/D-HCR structure Although a ganglioside binding site has never been unambiguously identified in BoNT/D-HCR a shallow cavity in an analogous location to the other BoNT serotypes HCR domains is observed in BoNT/D-HCR that has features compatible with membrane binding A portion of a loop near the putative receptor binding site K1236-N1244 is hydrophobic and solvent-exposed and may directly bind membrane lipids Liposome-binding experiments with BoNT/D-HCR demonstrate that this membrane lipid may be phosphatidylethanolamine (C) 2010 Elsevier Inc All rights reserved
