articleBiochemistryDec 17, 2005GREEN OA

Experimental Constraints on Quaternary Structure in Alzheimer's β-Amyloid Fibrils

National Institute of Diabetes and Digestive and Kidney Diseases · National Institutes of Health

PubMed
Indexed incrossrefpubmed

Abstract

We describe solid-state nuclear magnetic resonance (NMR) measurements on fibrils formed by the 40-residue beta-amyloid peptide associated with Alzheimer's disease (Abeta(1-40)) that place constraints on the identity and symmetry of contacts between in-register, parallel beta-sheets in the fibrils. We refer to these contacts as internal and external quaternary contacts, depending on whether they are within a single molecular layer or between molecular layers. The data include (1) two-dimensional 13C-13C NMR spectra that indicate internal quaternary contacts between side chains of L17 and F19 and side chains of I32, L34, and V36, as well as external quaternary contacts between side chains of I31 and G37; (2)…

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1,048
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23.10
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100%
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Authors

3

Topics & keywords

Keywords
  • Salt bridge
  • Side chain
  • Chemistry
  • Crystallography
  • Protein quaternary structure
  • Solid-state nuclear magnetic resonance
  • Molecular dynamics
  • Carboxylate
UN Sustainable Development Goals
  • Affordable and clean energy
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