Glycoproteomics Landscape of Asymptomatic and Symptomatic Human Alzheimer’s Disease Brain

• Published in: Molecular & cellular proteomics Vol. 21; no. 12; p. 100433
• Main Authors: Suttapitugsakul, Suttipong, Stavenhagen, Kathrin, Donskaya, Sofia, Bennett, David A., Mealer, Robert G., Seyfried, Nicholas T., Cummings, Richard D.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2022; American Society for Biochemistry and Molecular Biology
• Subjects: Alzheimer Disease - metabolism; Alzheimer’s disease; asymptomatic; Brain - metabolism; Glycoproteins - metabolism; glycoproteomics; Glycosylation; Humans; lectin enrichment; N-linked glycosylation; Polysaccharides - metabolism; Proteome - metabolism; symptomatic; glycoproteomics; APP; AD; Alzheimer’s disease; TBS; asymptomatic; SNA; SPE; WGA; Aβ; RCA; symptomatic; FDR; N-linked glycosylation; HILIC; lectin enrichment; ConA
• ISSN: 1535-9476; 1535-9484; 1535-9484
• DOI: 10.1016/j.mcpro.2022.100433

Molecular changes in the brain of individuals afflicted with Alzheimer's disease (AD) are an intense area of study. Little is known about the role of protein abundance and posttranslational modifications in AD progression and treatment, in particular large-scale intact N-linked glycoproteomics analysis. To elucidate the N-glycoproteome landscape, we developed an approach based on multi-lectin affinity enrichment, hydrophilic interaction chromatography, and LC-MS–based glycoproteomics. We analyzed brain tissue from 10 persons with no cognitive impairment or AD, 10 with asymptomatic AD, and 10 with symptomatic AD, detecting over 300 glycoproteins and 1900 glycoforms across the samples. The majority of glycoproteins have N-glycans that are high-mannosidic or complex chains that are fucosylated and bisected. The Man5 N-glycan was found to occur most frequently at >20% of the total glycoforms. Unlike the glycoproteomes of other tissues, sialylation is a minor feature of the brain N-glycoproteome, occurring at <9% among the glycoforms. We observed AD-associated differences in the number of antennae, frequency of fucosylation, bisection, and other monosaccharides at individual glycosylation sites among samples from our three groups. Further analysis revealed glycosylation differences in subcellular compartments across disease stage, including glycoproteins in the lysosome frequently modified with paucimannosidic glycans. These results illustrate the N-glycoproteomics landscape across the spectrum of AD clinical and pathologic severity and will facilitate a deeper understanding of progression and treatment development. [Display omitted] •Glycoproteomics analysis of human brains over stages of Alzheimer’s disease.•Enrichment of N-glycoproteins by multi-lectins and HILIC purification.•High-mannose and complex glycans that are fucosylated and bisected are predominant.•Site-specific variation of protein glycosylation among different AD stages. Glycosylation of proteins in human brains, especially those with Alzheimer’s disease (AD) is not well-known. We employed multi-lectin enrichment, HILIC, and mass spectrometry–based proteomics to profile N-glycoproteins in normal, asymptomatic, and symptomatic AD brains. Unlike other organs, the brain consists of mostly high-mannosidic glycans, notably the Man5 N-glycans and complex N-glycans that are fucosylated and bisected. We observed site-specific differences in glycosylation among different AD stages, such as the number of antennae or the frequency of fucosylation.