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Structures of engineered Clostridium botulinum neurotoxin derivatives


Reference:

Masuyer, G., Stancombe, P., Chaddock, J. A. and Acharya, K. R., 2011. Structures of engineered Clostridium botulinum neurotoxin derivatives. Acta Crystallographica Section F-Structural Biology and Crystallization Communications, 67 (12), pp. 1466-1472.

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Official URL:

http://dx.doi.org/10.1107/s1744309111034671

Abstract

Targeted secretion inhibitors (TSIs) are a new class of engineered biopharmaceutical molecules derived from the botulinum neurotoxins (BoNTs). They consist of the metalloprotease light chain (LC) and translocation domain (Hn) of BoNT; they thus lack the native toxicity towards motor neurons but are able to target soluble N-ethylmaleimide-sensitive fusion protein attachment receptor (SNARE) proteins. These functional fragment (LHn) derivatives are expressed as single-chain proteins and require post-translational activation into di-chain molecules for function. A range of BoNT derivatives have been produced to demonstrate the successful use of engineered SNARE substrate peptides at the LC-Hn interface that gives these molecules self-activating capabilities. Alternatively, recognition sites for specific exoproteases can be engineered to allow controlled activation. Here, the crystal structures of three LHn derivatives are reported between 2.7 and 3.0 angstrom resolution. Two of these molecules are derivatives of serotype A that contain a SNARE peptide. Additionally, a third structure corresponds to LHn serotype B that includes peptide linkers at the exoprotease activation site. In all three cases the added engineered segments could not be modelled owing to disorder. However, these structures highlight the strong interactions holding the LHn fold together despite the inclusion of significant polypeptide sequences at the LCHn interface.

Details

Item Type Articles
CreatorsMasuyer, G., Stancombe, P., Chaddock, J. A. and Acharya, K. R.
DOI10.1107/s1744309111034671
DepartmentsFaculty of Science > Biology & Biochemistry
RefereedYes
StatusPublished
ID Code27984

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