2VUA

Crystal Structure of the Botulinum Neurotoxin Serotype A binding domain

Summary for 2VUA

• Entry DOI: 10.2210/pdb2vua/pdb
• Related: 1UEE 2VU9 3BTA
• Descriptor: BOTULINUM NEUROTOXIN A HEAVY CHAIN (2 entities in total)
• Functional Keywords: ganglioside, receptor, toxin, membrane, secreted, metal-binding, hydrolase, metalloprotease, neurotoxin, protease
• Biological source: CLOSTRIDIUM BOTULINUM
• Total number of polymer chains: 1
• Total formula weight: 51713.40

Authors

Stenmark, P.,Dupuy, J.,Stevens, R.C. (deposition date: 2008-05-22, release date: 2008-08-26, Last modification date: 2023-12-13)

Primary citation

Stenmark, P.,Dupuy, J.,Imamura, A.,Kiso, M.,Stevens, R.C.
Crystal Structure of Botulinum Neurotoxin Type a in Complex with the Cell Surface Co-Receptor Gt1B- Insight Into the Toxin-Neuron Interaction.
Plos Pathog., 4:E129-, 2008

PubMed Abstract: Botulinum neurotoxins have a very high affinity and specificity for their target cells requiring two different co-receptors located on the neuronal cell surface. Different toxin serotypes have different protein receptors; yet, most share a common ganglioside co-receptor, GT1b. We determined the crystal structure of the botulinum neurotoxin serotype A binding domain (residues 873-1297) alone and in complex with a GT1b analog at 1.7 A and 1.6 A, respectively. The ganglioside GT1b forms several key hydrogen bonds to conserved residues and binds in a shallow groove lined by Tryptophan 1266. GT1b binding does not induce any large structural changes in the toxin; therefore, it is unlikely that allosteric effects play a major role in the dual receptor recognition. Together with the previously published structures of botulinum neurotoxin serotype B in complex with its protein co-receptor, we can now generate a detailed model of botulinum neurotoxin's interaction with the neuronal cell surface. The two branches of the GT1b polysaccharide, together with the protein receptor site, impose strict geometric constraints on the mode of interaction with the membrane surface and strongly support a model where one end of the 100 A long translocation domain helix bundle swing into contact with the membrane, initiating the membrane anchoring event.

PubMed: 18704164
DOI: 10.1371/JOURNAL.PPAT.1000129

Experimental method

X-RAY DIFFRACTION (1.7 Å)