N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein

N-β-methylamino-L-alanine (BMAA) is a naturally-occurring toxin produced in cyanobacteria that has been linked to neurological degeneration. Efforts to study and quantify BMAA in the environment are hampered by two biologically-occurring isomers, N-(2- aminoethyl)glycine (AEG) and 2,4-diaminobutyric...

Full description

Bibliographic Details
Main Author: Glover, William Broc
Language:English
Published: University of British Columbia 2014
Online Access:http://hdl.handle.net/2429/50730
id ndltd-UBC-oai-circle.library.ubc.ca-2429-50730
record_format oai_dc
spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-507302018-01-05T17:27:44Z N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein Glover, William Broc N-β-methylamino-L-alanine (BMAA) is a naturally-occurring toxin produced in cyanobacteria that has been linked to neurological degeneration. Efforts to study and quantify BMAA in the environment are hampered by two biologically-occurring isomers, N-(2- aminoethyl)glycine (AEG) and 2,4-diaminobutyric acid (DAB), that exist in very low concentrations in many sample matrices, indicating a need for improved analytical methods. The first objective of this thesis is to develop an accurate, precise and sensitive method for the analysis of BMAA and the isomers AEG and DAB that is applicable to a wide variety of sample matrices. A method for complete chromatographic separation of the isomers was developed using chemical derivatization, reversed phase chromatography and tandem mass spectrometry, and was validated with cyanobacteria-containing natural health products. The mechanism of toxicity of BMAA is not fully understood, and previous studies have shown an association between BMAA and protein. The second objective of this thesis is to determine whether BMAA is incorporated into protein via a modified proteomics approach used to identify peptides containing BMAA in tissue from post-mortem human patients. This approach identified BMAA in proteins isolated from the frontal lobe of Amyotrophic Lateral Sclerosis (ALS), Alzheimer’s disease (AD), and control patients. To determine whether BMAA incorporation into protein occurs as an error in synthesis, a cell-free expression system was challenged with a deficiency of specific amino acids and supplemented with BMAA. BMAA was incorporated into protein via an error in synthesis. Together, these data demonstrate accurate methods for quantification of BMAA, a route of exposure through dietary products, and a potential mechanism for storage of BMAA in proteins. Irving K. Barber School of Arts and Sciences (Okanagan) Biology, Department of (Okanagan) Graduate 2014-10-14T19:42:20Z 2014-10-14T19:42:20Z 2014 2014-09 Text Thesis/Dissertation http://hdl.handle.net/2429/50730 eng Attribution-NonCommercial-NoDerivs 2.5 Canada http://creativecommons.org/licenses/by-nc-nd/2.5/ca/ University of British Columbia
collection NDLTD
language English
sources NDLTD
description N-β-methylamino-L-alanine (BMAA) is a naturally-occurring toxin produced in cyanobacteria that has been linked to neurological degeneration. Efforts to study and quantify BMAA in the environment are hampered by two biologically-occurring isomers, N-(2- aminoethyl)glycine (AEG) and 2,4-diaminobutyric acid (DAB), that exist in very low concentrations in many sample matrices, indicating a need for improved analytical methods. The first objective of this thesis is to develop an accurate, precise and sensitive method for the analysis of BMAA and the isomers AEG and DAB that is applicable to a wide variety of sample matrices. A method for complete chromatographic separation of the isomers was developed using chemical derivatization, reversed phase chromatography and tandem mass spectrometry, and was validated with cyanobacteria-containing natural health products. The mechanism of toxicity of BMAA is not fully understood, and previous studies have shown an association between BMAA and protein. The second objective of this thesis is to determine whether BMAA is incorporated into protein via a modified proteomics approach used to identify peptides containing BMAA in tissue from post-mortem human patients. This approach identified BMAA in proteins isolated from the frontal lobe of Amyotrophic Lateral Sclerosis (ALS), Alzheimer’s disease (AD), and control patients. To determine whether BMAA incorporation into protein occurs as an error in synthesis, a cell-free expression system was challenged with a deficiency of specific amino acids and supplemented with BMAA. BMAA was incorporated into protein via an error in synthesis. Together, these data demonstrate accurate methods for quantification of BMAA, a route of exposure through dietary products, and a potential mechanism for storage of BMAA in proteins. === Irving K. Barber School of Arts and Sciences (Okanagan) === Biology, Department of (Okanagan) === Graduate
author Glover, William Broc
spellingShingle Glover, William Broc
N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein
author_facet Glover, William Broc
author_sort Glover, William Broc
title N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein
title_short N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein
title_full N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein
title_fullStr N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein
title_full_unstemmed N-beta-methylamino-L-alanine : a non-protein amino acid incorporated into protein
title_sort n-beta-methylamino-l-alanine : a non-protein amino acid incorporated into protein
publisher University of British Columbia
publishDate 2014
url http://hdl.handle.net/2429/50730
work_keys_str_mv AT gloverwilliambroc nbetamethylaminolalanineanonproteinaminoacidincorporatedintoprotein
_version_ 1718584479327453184