Experimental Constraints on Quaternary Structure in Alzheimer's β-Amyloid Fibrils
National Institute of Diabetes and Digestive and Kidney Diseases · National Institutes of Health
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)…
Citation impact
- FWCI
- 23.10
- Percentile
- 100%
- References
- 93
Authors
3- ATAneta T. PetkovaCorresponding
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
- WYWai‐Ming Yau
National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
- RTRobert Tycko
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Topics & keywords
- Salt bridge
- Side chain
- Chemistry
- Crystallography
- Protein quaternary structure
- Solid-state nuclear magnetic resonance
- Molecular dynamics
- Carboxylate
- Affordable and clean energy