Generation and study of antibodies against two triangular trimers derived from Aβ

Adam G. Kreutzer, Ryan J. Malonis, Chelsea Marie T. Parrocha, Karen Tong, Gretchen Guaglianone, Jennifer T. Nguyen, Michelle N. Diab, Jonathan R. Lai, James S. Nowick

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Monoclonal antibodies (mAbs) that target the β-amyloid peptide (Aβ) are important Alzheimer's disease research tools and are now being used as Alzheimer's disease therapies. Conformation-specific mAbs that target oligomeric and fibrillar Aβ assemblies are of particular interest, as these assemblies are associated with Alzheimer's disease pathogenesis and progression. This article reports the generation of rabbit mAbs against two different triangular trimers derived from Aβ. These antibodies are the first mAbs generated against Aβ oligomer mimics in which the high-resolution structures of the oligomers are known. We describe the isolation of the mAbs using single B-cell sorting of peripheral blood mononuclear cells (PBMCs) from immunized rabbits, the selectivity of the mAbs for the triangular trimers, the immunoreactivity of the mAbs with aggregated Aβ42, and the immunoreactivity of the mAbs in brain tissue from the 5xFAD Alzheimer's disease mouse model. The characterization of these mAbs against structurally defined trimers derived from Aβ enhances understanding of antibody-amyloid recognition and may benefit the development of diagnostics and immunotherapies in Alzheimer's disease.

Original languageEnglish (US)
Article numbere24333
JournalPeptide Science
Volume116
Issue number2
DOIs
StatePublished - Mar 2024

Keywords

  • Alzheimer's disease
  • X-ray crystallography
  • amyloid oligomers
  • monoclonal antibodies

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Biomaterials
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Generation and study of antibodies against two triangular trimers derived from Aβ'. Together they form a unique fingerprint.

Cite this