Eri Saijo

ORCID: 0000-0002-2047-2000
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Prion Diseases and Protein Misfolding
  • Neurological diseases and metabolism
  • Plant Reproductive Biology
  • Enzyme Structure and Function
  • Alzheimer's disease research and treatments
  • Trace Elements in Health

Colorado State University
2012-2021

University of Kentucky
2011-2013

Prions are infectious proteins causing fatal, transmissible neurodegenerative diseases of animals and humans. Replication involves template-directed refolding host encoded prion protein, PrP C , by its conformation, Sc . Following discovery in captive Colorado deer 1967, uncontrollable contagious transmission chronic wasting disease (CWD) led to an expanded geographic range increasing numbers free-ranging North American (NA) cervids. Some five decades later, detection Norwegian (NO) reindeer...

10.1371/journal.ppat.1009748 article EN cc-by PLoS Pathogens 2021-07-26

Whereas prion replication involves structural rearrangement of cellular protein (PrP(C)), the existence conformational epitopes remains speculative and controversial, PrP transformation is monitored by immunoblot detection PrP(27-30), a protease-resistant counterpart pathogenic scrapie form (PrP(Sc)) PrP. We now describe involvement specific amino acids in determinants novel monoclonal antibodies (mAbs) raised against randomly chimeric Epitope recognition two mAbs depended on polymorphisms...

10.1074/jbc.m112.395921 article EN cc-by Journal of Biological Chemistry 2012-09-05

Although they share certain biological properties with nucleic acid based infectious agents, prions, the causative agents of invariably fatal, transmissible neurodegenerative disorders such as bovine spongiform encephalopathy, sheep scrapie, and human Creutzfeldt Jakob disease, propagate by conformational templating host encoded proteins. Once thought to be unique these diseases, this mechanism is now recognized a ubiquitous means information transfer in systems, including other protein...

10.1371/journal.ppat.1003692 article EN cc-by PLoS Pathogens 2013-10-31

The suggested role of cellular prion protein (PrP (C) ) in mediating the toxic effects oligomeric amyloid β peptide (Aβ) Alzheimer disease (AD) is controversial. To address hypothesis that variable PrP expression involved AD pathogenesis, we analyzed PrPC frontal and temporal cortices hippocampus individuals with no cognitive impairment (NCI), amnestic mild (aMCI), (mAD), AD. We found all brain regions was not significantly altered among various patient groups. In addition, levels groups did...

10.4161/pri.5.2.16355 article EN Prion 2011-04-01
Coming Soon ...