Beta-amyloid (A?) is the primary protein component of Alzheimer's disease (AD) amyloid plaques, and there is substantial evidence to support the hypothesis that soluble A? aggregates are neurotoxic. Transgenic mice expressing the Swedish mutation of the human A? precursor protein (APPSw) produce high levels of A? and develop amyloid plaques, but surprisingly they do not suffer the extensive neuronal cell death characteristic of AD. Recent studies have uncovered a possible explanation: APPSw mice upregulate synthesis of transthyretin (TTR), a transport protein found in plasma and cerebrospinal fluid, and TTR appears to protect the mice from the neurotoxic effects of A?. The long-term goals of this project are to answer three questions that arise from this intriguing discovery: (1) how does TTR exert its protective activity? (2) why does this natural protective activity fail in AD? (3) can it be restored or replaced? In aim 1, the specific residues on TTR involved with binding to A? will be identified. From mass spectrometry analysis coupled with peptide array binding studies, residues on the G strand and near the EF helix of TTR were implicated. Further definition of the binding site will be obtained by screening for A? binding to peptide library derived from overlapping sequences of TTR, and by targeted alanine mutagenesis. Compounds that mimic the TTR binding sites will be synthesized and tested for A? binding as well as inhibition of in vitro toxicity.
In aim 2, the effect of TTR and variants on ? aggregation will be characterized. Preliminary data show that TTR quaternary structure and stability, oxidation, and binding of natural ligands all influence the extent of A? binding to TTR. The greatest A? binding is observed at intermediate aggregation states. Put another way, TTR may be a natural scavenger for the most toxic A? aggregates. Aggregation of A? in the presence of TTR will be characterized by a combination of dynamic and static light scattering, and nanoparticle tracking. These complementary methods, which are particularly suited for examining soluble aggregates, will yield data on aggregate size, size distribution, number, morphology, and aggregation rate. Synthetic mimics, developed in aim 1, will also be characterized for their effect on A? aggregation.
In aim 3, further validation of TTR's neuroprotective action will be sought. Astrocytes will be transfected to secrete TTR (wt and monomeric), and inhibition of A? toxicity will be tested in vitro with mixed cortical cultures, or y adding medium from secreting astrocytes to highly enriched cortical neurons. Transgenic mice that overexpress TTR in astrocytes on an APP/PS1 background will be generated, and pathological endpoints will be evaluated to ascertain the level of in vivo protection afforded by TTR. Finally, initial screening of promising TTR mimics from Aim 1 will be tested in a stereotactic injection assay. These studies, which integrate chemical, biophysical, and biological approaches, will provide a rational basis for developing novel pharmacological approaches to preventing AD by enhancement of TTR's natural defenses.

Public Health Relevance

Alzheimer's disease has been linked to deposition of beta-amyloid plaques in the brain and subsequent death of neurons. Studies with transgenic mice suggest that a normal protein, transthyretin may provide some protection against the neuronal cell death caused by beta-amyloid. This investigation will provide a rational basis for elucidating why this protective action of TTR is lost and for developing novel pharmacological approaches to preventing Alzheimer's disease by restoration or replacement of the natural defenses provided by transthyretin.

National Institute of Health (NIH)
National Institute on Aging (NIA)
Research Project (R01)
Project #
Application #
Study Section
Biophysics of Neural Systems Study Section (BPNS)
Program Officer
Yang, Austin Jyan-Yu
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of Wisconsin Madison
Engineering (All Types)
Biomed Engr/Col Engr/Engr Sta
United States
Zip Code
Pate, Kayla M; Kim, Brandon J; Shusta, Eric V et al. (2018) Transthyretin Mimetics as Anti-?-Amyloid Agents: A?Comparison of Peptide and Protein Approaches. ChemMedChem 13:968-979
Lu, Xiaomeng; Murphy, Regina M (2018) Nanoparticle Tracking for Protein Aggregation Research. Methods Mol Biol 1777:145-158
Pate, Kayla M; Murphy, Regina M (2017) Cerebrospinal Fluid Proteins as Regulators of Beta-amyloid Aggregation and Toxicity. Isr J Chem 57:602-612
Lu, Xiaomeng; Brickson, Claire R; Murphy, Regina M (2016) TANGO-Inspired Design of Anti-Amyloid Cyclic Peptides. ACS Chem Neurosci 7:1264-74
Mangrolia, Parth; Yang, Dennis T; Murphy, Regina M (2016) Transthyretin variants with improved inhibition of ?-amyloid aggregation. Protein Eng Des Sel 29:209-218
Johnson, Delinda A; Johnson, Jeffrey A (2015) Nrf2--a therapeutic target for the treatment of neurodegenerative diseases. Free Radic Biol Med 88:253-267
Cho, Patricia Y; Joshi, Gururaj; Boersma, Melissa D et al. (2015) A Cyclic Peptide Mimic of the ?-Amyloid Binding Domain on Transthyretin. ACS Chem Neurosci 6:778-89
Yang, Dennis T; Lu, Xiaomeng; Fan, Yamin et al. (2014) Evaluation of Nanoparticle Tracking for Characterization of Fibrillar Protein Aggregates. AIChE J 60:1236-1244
Cho, Patricia Y; Joshi, Gururaj; Johnson, Jeffrey A et al. (2014) Transthyretin-derived peptides as ?-amyloid inhibitors. ACS Chem Neurosci 5:542-51
Yang, Dennis T; Joshi, Gururaj; Cho, Patricia Y et al. (2013) Transthyretin as both a sensor and a scavenger of ?-amyloid oligomers. Biochemistry 52:2849-61

Showing the most recent 10 out of 12 publications