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Antibody against Small Aggregated Peptide Specifically Recognizes Toxic Aβ-42 Oligomers in Alzheimer's Disease

  • Mitchell Center for Neurodegenerative Diseases, Galveston
    ,
  • Department of Pharmacology and Toxicology, Galveston
Research Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Publication metrics

Metrics

SciVal
Citations
20
SciVal
FWCI
0.89
SciVal
Author count
7
SciVal
Paper percentile
68
Scopus
Citations

Abstract

Amyloid-beta (Aβ) oligomers have emerged as the most toxic species in Alzheimer's disease (AD) and other amyloid pathologies. Also, Aβ-42 peptide is more aggregation-prone compared to other Aβ isoforms. Thus, we synthesized a small peptide of repeated sequence containing the last three amino acids, Val-40, Ile-41, and Ala-42 of Aβ-42 that was subsequently aggregated and used to generate a novel antibody, VIA. In this study, we examined human AD and Tg2576 mouse brain samples using VIA in combination with other amyloid-specific antibodies and confirmed the specificity of VIA to oligomeric Aβ-42. Moreover, we found that VIA does not recognize classic amyloid plaques composed of fibrillar Aβ or Aβ-40 ex vivo. Since VIA recognizes a distinct epitope specific to Aβ-42 oligomers, it may have broad use for examining the accumulation of these oligomers in AD and other neurodegenerative diseases. VIA may also be used in immunotherapy studies to prevent neurodegenerative effects associated with Aβ-42 oligomers.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 1981-1989 (9 pages)

Journal (Volume, Issue Number)

ACS Chemical Neuroscience (Volume 6, Issue 12)

Publication milestones

  • Published - 16/12/2015

Publication status

Published - 16/12/2015

ISSN

1948-7193

Publication IDs

  • ORCID: /0000-0003-2511-949X/work/43281169
  • Scopus: 84950288771
  • WOS: 000366884500010