Methods for the Chemical Analysis of β-N-Methylamino-L-A lanine: What Is Known and What Remains to Be Determined

Neurotox Res. 2018 Jan;33(1):184-191. doi: 10.1007/s12640-017-9744-7. Epub 2017 May 4.

Abstract

β-N-Methylamino-L-alanine (BMAA) is a non-canonical amino acid implicated as a cause for amyotrophic lateral sclerosis/parkinsonism dementia complex and potentially other neurodegenerative diseases. As interest in this molecule has increased, there has been a proliferation of methods along with a plethora of opinions as to the superiority of some methods over others. We analyzed the literature with reference to BMAA and its naturally occurring isomers, N-(2-aminoethyl) glycine (AEG) and 2,4 diaminobutyric acid (DAB). A comparison of methods, results, and critiques reveal that a single method has been approved by the AOAC but several different methods provide comparable BMAA quantification concentrations in similar tissues. We also describe a productive way to move forward as technology improves and changes.

Keywords: 6-Aminoquinolyl-N-hydroxysuccinimidyl carbamate; AOAC; AQC; Analytical chemistry; BMAA; HILIC; Methods.

Publication types

  • Review

MeSH terms

  • Amino Acids, Diamino / analysis*
  • Amino Acids, Diamino / chemistry
  • Animals
  • Chromatography, Liquid
  • Cyanobacteria Toxins
  • Neurotoxins / analysis*
  • Neurotoxins / chemistry
  • Reproducibility of Results
  • Tandem Mass Spectrometry

Substances

  • Amino Acids, Diamino
  • Cyanobacteria Toxins
  • Neurotoxins
  • beta-N-methylamino-L-alanine