Crystal structures of <scp>OrfX1</scp>, <scp>OrfX2</scp> and the <scp>OrfX1</scp>–<scp>OrfX3</scp> complex from the <scp><i>orfX</i></scp> gene cluster of botulinum neurotoxin <scp>E1</scp>

Linfeng Gao(University of California, Irvine), Kwok Ho Lam(University of California, Irvine), Shun Liu(University of California, Irvine), Adina Przykopanski(Medizinische Hochschule Hannover), Johanna Lübke(Medizinische Hochschule Hannover), Ruifeng Qi(University of California, Irvine), Maren Krüger(Robert Koch Institute), Maria B. Nowakowska(University of Helsinki), Katja Selby(University of Helsinki), François P. Douillard(University of Helsinki), Martin B. Dorner(Robert Koch Institute), Kay Perry(Argonne National Laboratory), Miia Lindström(University of Helsinki), Brigitte G. Dorner(Robert Koch Institute), Andreas Rummel(Medizinische Hochschule Hannover), Rongsheng Jin(University of California, Irvine)
FEBS Letters
January 19, 2023
Cited by 11Open Access
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Abstract

Botulinum neurotoxins (BoNTs) are among the most lethal toxins known to humans, comprising seven established serotypes termed BoNT/A-G encoded in two types of gene clusters (ha and orfX) in BoNT-producing clostridia. The ha cluster encodes four non-toxic neurotoxin-associated proteins (NAPs) that assemble with BoNTs to protect and enhance their oral toxicity. However, the structure and function of the orfX-type NAPs remain largely unknown. Here, we report the crystal structures for OrfX1, OrfX2, and an OrfX1-OrfX3 complex, which are encoded in the orfX cluster of a BoNT/E1-producing Clostridium botulinum strain associated with human foodborne botulism. These structures lay the foundation for future studies on the potential roles of OrfX proteins in oral intoxication and pathogenesis of BoNTs.


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