Amyloid deposits found in neurodegenerative diseases result from misfolding of cellular proteins. The challenge for developing specific inhibitors that block oligomer or fibril formation is that there are no high- resolution molecular structures that can guide the design. The proposal has three specific aims.
The first aim i s to use high-resolution solid-state NMR in combination with atomic force microscopy (AFM) to refine the structures that are emerging of Abeta oligomers and fibrils.
The second aim i s to design inhibitors based on the structural data from Aim 1 and to test their ability in vitro to block oligomer or fibril formation.
The third aim i s to assay the ability of these inhibitors to block the toxicity of Abeta oligomers and fibrils on neuronal cells. ? ? A new approach has been developed for obtaining high-resolution AFM images of Abeta soluble oligomers and fibrils in solution. The method takes advantage of a novel AFM controller that provides resolution in 'single touch' AFM experiments that surpasses the resolution currently available using commercial instruments. High resolution AFM of solution samples will allow us to follow the formation of Abeta oligomers, protofibrils and fibrils, and determine how designed inhibitors prevent fibrillization. ? ? We have developed structural models for the Abeta42 monomer, dimer, protofibril and fibril based on preliminary results from high resolution AFM and solid-state NMR. The structures show that when the b-strands have a parallel orientation and the amino acids are in-register with one another, the surface of the b-sheet has pronounced ridges and grooves. This architecture provides the key elements for the rational design of inhibitors to prevent fibril formation. Our template inhibitor peptide based on a rational design approach has the sequence GxFxGxF, where the bulky phenylalanine side chains of the inhibitor are predicted to pack against the glycines in the GxxxG motif of the amyloidogenic peptide. ? ? We will test the ability of the designed peptides to disrupt the formation of oligomers and fibrils by thioflavin T fluorescence, size exclusion chromatography, electron microscopy, AFM and solid-state NMR. We will also test the ability of our designed inhibitors to protect neurons from cell death induced by amyloid fibrils. We will focus on the Abeta42 peptide because of its higher ability to form aggregates than the shorter isoforms. Moreover, most gene mutations that are associated with the inherited forms of Alzheimer's disease result in an increase in the ratio of Abeta42 over Abeta40. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG027317-03
Application #
7414539
Study Section
Special Emphasis Panel (ZRG1-MDCN-C (95))
Program Officer
Snyder, Stephen D
Project Start
2006-09-01
Project End
2011-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
3
Fiscal Year
2008
Total Cost
$282,825
Indirect Cost
Name
State University New York Stony Brook
Department
Biochemistry
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Decock, Marie; Stanga, Serena; Octave, Jean-Noël et al. (2016) Glycines from the APP GXXXG/GXXXA Transmembrane Motifs Promote Formation of Pathogenic A? Oligomers in Cells. Front Aging Neurosci 8:107
Decock, Marie; El Haylani, Laetitia; Stanga, Serena et al. (2015) Analysis by a highly sensitive split luciferase assay of the regions involved in APP dimerization and its impact on processing. FEBS Open Bio 5:763-73
Fu, Ziao; Aucoin, Darryl; Davis, Judianne et al. (2015) Mechanism of Nucleated Conformational Conversion of A?42. Biochemistry 54:4197-207
Marinangeli, Claudia; Tasiaux, Bernadette; Opsomer, Rémi et al. (2015) Presenilin transmembrane domain 8 conserved AXXXAXXXG motifs are required for the activity of the ?-secretase complex. J Biol Chem 290:7169-84
Xu, Feng; Kotarba, AnnMarie E; Ou-Yang, Ming-Hsuan et al. (2014) Early-onset formation of parenchymal plaque amyloid abrogates cerebral microvascular amyloid accumulation in transgenic mice. J Biol Chem 289:17895-908
Tang, Tzu-Chun; Hu, Yi; Kienlen-Campard, Pascal et al. (2014) Conformational changes induced by the A21G Flemish mutation in the amyloid precursor protein lead to increased A? production. Structure 22:387-96
Kotarba, Annmarie E; Aucoin, Darryl; Hoos, Michael D et al. (2013) Fine mapping of the amyloid ýý-protein binding site on myelin basic protein. Biochemistry 52:2565-73
Ladiwala, Ali Reza A; Litt, Jeffrey; Kane, Ravi S et al. (2012) Conformational differences between two amyloid ? oligomers of similar size and dissimilar toxicity. J Biol Chem 287:24765-73
Liao, Mei-Chen; Hoos, Michael D; Aucoin, Darryl et al. (2010) N-terminal domain of myelin basic protein inhibits amyloid beta-protein fibril assembly. J Biol Chem 285:35590-8
Ahmed, Mahiuddin; Davis, Judianne; Aucoin, Darryl et al. (2010) Structural conversion of neurotoxic amyloid-beta(1-42) oligomers to fibrils. Nat Struct Mol Biol 17:561-7

Showing the most recent 10 out of 16 publications