Exploring the brain tissue proteome of TgCRND8 Alzheimer's Disease model mice under B vitamin deficient diet induced hyperhomocysteinemia by LC-MS top-down platform.
Alzheimer Disease
/ genetics
Amyloid beta-Peptides
/ metabolism
Animals
Brain
/ metabolism
Brain Chemistry
Calmodulin-Binding Proteins
/ genetics
Chromatography, Liquid
Cytoskeletal Proteins
/ genetics
Disease Models, Animal
Female
Humans
Hyperhomocysteinemia
/ etiology
Male
Mass Spectrometry
Metallothionein 3
Mice
Mice, Transgenic
Nerve Tissue Proteins
/ genetics
Proteome
/ chemistry
Vitamin B Complex
/ analysis
Alzheimer's Disease
Diet
Mass spectrometry, Personalized medicine
TgCRND8 mice
Top down proteomics
Journal
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
ISSN: 1873-376X
Titre abrégé: J Chromatogr B Analyt Technol Biomed Life Sci
Pays: Netherlands
ID NLM: 101139554
Informations de publication
Date de publication:
15 Aug 2019
15 Aug 2019
Historique:
received:
14
01
2019
revised:
28
05
2019
accepted:
04
06
2019
pubmed:
16
6
2019
medline:
18
12
2019
entrez:
16
6
2019
Statut:
ppublish
Résumé
The multifactorial nature of Late Onset Alzheimer's Disease (LOAD), the AD form of major relevance on epidemiological and social aspects, has driven the original investigation by LC-MS and top-down proteomics approach of the protein repertoire of the brain tissue of TgCRND8 model mice fed with a diet deficient in B vitamins. The analysis of the acid-soluble fraction of brain tissue homogenates identified a list of proteins and peptides, proteoforms and PTMs. In order to disclose possible modulations, their relative quantification in wild type and AD model mice under both B vitamin deficient and control diets was performed. The levels of metallothionein III, guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 and brain acid soluble protein 1 showed statistically significant alterations depending on genotype, diet or both effects, respectively. Particularly, metallothionein III exhibited increased levels in TgCRND8 mice under B vitamin deficient diet with respect to wild type mice under both diets. Brain acid soluble protein 1 showed the opposite, revealing decreased levels in all diet groups of AD model mice with respect to wild type mice in control diet. Lower levels of brain acid soluble protein 1 were also observed in wild type mice under deficiency of B vitamins. These results, besides contributing to increase the knowledge of AD at molecular level, give new suggestions for deeply investigating metallothionein III and brain acid soluble protein 1 in AD.
Identifiants
pubmed: 31202182
pii: S1570-0232(19)30081-9
doi: 10.1016/j.jchromb.2019.06.005
pii:
doi:
Substances chimiques
Amyloid beta-Peptides
0
Basp1 protein, mouse
0
Calmodulin-Binding Proteins
0
Cytoskeletal Proteins
0
Metallothionein 3
0
Nerve Tissue Proteins
0
Proteome
0
Vitamin B Complex
12001-76-2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
165-172Informations de copyright
Copyright © 2019. Published by Elsevier B.V.