Improved detection of botulinum type E by rational design of a new peptide substrate for endopeptidase-mass spectrometry assay

Anal Biochem. 2014 Jul 1:456:50-2. doi: 10.1016/j.ab.2014.03.024. Epub 2014 Apr 8.

Abstract

Botulinum neurotoxins (BoNTs) are the most toxic substances known to humans. Endopeptidase-mass spectrometry (Endopep-MS) is used as a specific and rapid in vitro assay to detect BoNTs. In this assay, immunocaptured toxin cleaves a serotype-specific peptide substrate, and the cleavage products are then detected by MS. To further improve the sensitivity of the assay, we report here the rational design of a new substrate peptide for the detection of botulinum neurotoxin type E (BoNT/E). Our strategy was based on previously reported structural interactions integrated with analysis method efficiency considerations. Integration of the newly designed substrate has led to a more than one order of magnitude increased sensitivity of the assay.

Keywords: Botulinum neurotoxin; Detection; Mass spectrometry; Peptide substrate; UPLC.

MeSH terms

  • Amino Acid Sequence
  • Botulinum Toxins / analysis*
  • Botulinum Toxins / metabolism*
  • Drug Design*
  • Immunoassay
  • Mass Spectrometry / methods*
  • Molecular Sequence Data
  • Peptides / chemistry
  • Peptides / metabolism*

Substances

  • Peptides
  • Botulinum Toxins
  • botulinum toxin type E