Dr. Carol Hall, Alcoa Professor of chemical engineering at NC State and Hung D. Nguyen, a graduate student in Hall's lab, used a computer simulation technique, discontinuous molecular dynamics, to visualize the meanderings of small proteins called peptides. Movies of the simulation show that 96 randomly placed peptides spontaneously aggregate into what Hall calls a "sandwich" of layered protein sheets, similar to the amyloid fibrils discovered in diseased people and animals. Hall says that understanding how fibrils form in human or animal organs may lead to discoveries of how to slow or halt fibril formation.
The research was published in the Nov. 16 edition of Proceedings of the National Academy of Sciences.
It is not known whether fibrils cause Alzheimer's, Parkinson's and the other so-called amyloid diseases, or whether they are just associated symptoms. In any event, the fibrils form plaques in human and animal organs, often the brain. Although it's not clear if these plaques cause memory loss in Alzheimer's patients, for instance, scientists are interested in finding out the mechanisms behind the formation of fibrils.
"All of these diseases - Alzheimer's, Parkinson's, ALS, Huntington's - have the same unusual phenomena. Proteins - completely different proteins in each disease - assemble into ordered aggregates, amyloid fibrils, so that a vital organ, usually the brain, is crisscrossed by these structures," Hall said. "This tells us that the problem has something to do with the general nature of proteins rather than with the specifics of the particular disease-associated proteins."
Besides studying fibrils in the test tube, researchers would like to make computer models to view fibril formation. This is not possible using the traditional atomic-level protein folding simulation techniques - which follow the motions of every atom on every protein - because fibril formation takes a long time.
So Hall and Nguyen developed a less-detailed model of protein geometry and energetics and applied it to a relatively simple protein, polyalanine, which had been found to form fibrils in test tubes. With this approach, the NC State researchers were able to watch spontaneous fibril formation in about 60 hours on a fast computer. That's much quicker than atomic-level simulations.
In the simulation movie, 12 to 96 peptides were initially scattered randomly across the computer screen. When set into motion, the researchers first saw groups of two to five proteins coming together and falling apart and eventually forming amorphous clumps that twist around each other, like a rope. These twisted structures began coming together, like the ingredients in a sandwich, layered above and below each other. In the end, the simulation showed a fibril-like structure with only a few outlying peptides refusing to aggregate.
Hall says her method of reducing the level of detail in her protein model just to the point where the key features that drive fibril formation remain and other features are neglected allows her to get a broad molecular-level picture of the fibril formation process.
Hall's work is sponsored by the National Institutes of Health. She has recently been funded to attempt computer simulations of fibril formation by beta amyloids, the peptides that aggregate in Alzheimer's disease.
Dr. Carol Hall, 919-515-3571
Mick Kulikowski, News Services, 919-515-3470
Note to editors: An abstract of the paper follows.
"Molecular Dynamic Simulations of Spontaneous Fibril Formation By Random-Coil Peptides"
Authors: Hung D. Nguyen and Dr. Carol Hall, North Carolina State University
Published: Nov. 16, 2004, in Proceedings of the National Academy of Sciences
Abstract: Assembly of normally soluble proteins into amyloid fibrils is a cause or associated symptom of numerous human disorders, including Alzheimer's and the prion diseases. We report molecular-level simulation of spontaneous fibril formation. Systems containing 12-96 model polyalanine peptides form fibrils at temperatures grater than a critical temperature that decreases with peptide concentration and exceeds the peptide's folding temperature, consistent with experimental findings. Formation of small amorphous aggregates precedes ordered nucleus formation and subsequent rapid fibril growth through addition of beta-sheets laterally and monomeric peptides at fibril ends. The fibril's structure is similar to that observed experimentally.