Dementia Today.net

Site updated at Wednesday, 22 June 2016

Living with Dementia

Alzheimer protein’s structure may explain its toxicity

  • - Dementia News
  • May 08, 2015
  • Comments
  • Viewed: 0
Tags: |

Researchers at the University of Illinois at Chicago have determined the molecular structure of one of the proteins in the fine fibers of the brain plaques that are a hallmark of Alzheimer’s disease. This molecule, called amyloid beta-42, is toxic to nerve cells and is believed to provoke the disease cascade.

The study is online in the journal Nature Structural and Molecular Biology.

Knowing the physical structure of the 42 amino acid-long form of amyloid beta in the fibers is key to understanding how it folds up improperly and aggregates into toxic plaques, says Yoshitaka Ishii, UIC professor of chemistry and principal investigator on the study.

Ishii and his colleagues found that amyloid beta-42 in amyloid fibrils forms three flat structures (called beta sheets) that turn back and forth to layer over each other in an"S” pattern. They also found that the final amino acid on the protein forms a “salt bridge” with an amino acid at the first turn of the S, stabilizing the structure. A salt bridge is a bond between positive- and negative-charged molecules or parts of a molecule.

The 3-D structure is strikingly different from that of amyloid beta-40, a chemically similar and more abundant protein also linked to Alzheimer’s. Amyloid beta-40 lacks the final amino acid that carries the negative charge needed to form the salt bridge.

“This explains why amyloid beta-42 doesn’t interact with amyloid beta-40, or recruit it into the plaques that are toxic to nerve cells,” Ishii said.

The structural features and folding behavior of amyloid beta-42 “offer a new perspective on amyloid propagation in Alzheimer’s disease and, perhaps, other neurodegenerative disease,” said Ishii. Drugs designed to act against amyloid beta-40, he said, “may not work well against the more toxic amyloid beta-42.”

The chemical nature of amyloid beta-42—especially its extreme aversion to water—posed a formidable challenge to chemists and structural biologists, Ishii said. “There are a number of laboratories that have been working on this problem, and I am very proud of the work of my graduate student Yiling Xiao in elucidating its structure.” Xiao is first author on the study.

###

Other authors are Dan McElheny, Sudhakar Parthasarathy, and Fei Long of UIC chemistry; Buyong Ma of the National Cancer Institute at Frederick, Maryland; Ruth Nussinov of the NCI and the Sackler School of Medicine in Tel Aviv; and Minako Hoshi of Kyoto University in Japan.

The work was supported primarily by a National Institutes of Health grant (GM 098033) and an Alzheimer’s Association Investigator-Initiated Research Grant (08-91256). Other support came from the NIH’s Frederick National Laboratory for Cancer Research under contract HHSN261200800001E and the NIH Intramural Research Program.

###

Jeanne Galatzer-Levy
.(JavaScript must be enabled to view this email address)
312-996-1583

University of Illinois at Chicago

Post a comment [ + Comment here + ]

There are no comments for this entry yet. [ + Comment here + ]




Comment
Your details

* Required field


Please enter the word you see in the image below:

Comments are moderated by our editors, so there may be a delay between submission and publication of your comment. Offensive or abusive comments will not be published.

Living With Dementia

brain changes1 - menopause1 - morphometry1 - magnetic resonance spectroscopy1 - type 1 diabetes1 - tau proteins1 - cholesterol1 - hypertension3 - vascular cognitive impairment1 - alzheimer's disease symptoms1 - pd with dementia1 - bapineuzumab1 - alzheimers association1 - neurofibrillary tangles3 - brewer1 - sanofi1 - beta secretase1 - neurologic disorder1 - pre-dementia stage1 - aβ421 - korsakoff's syndrome10 - social engagement1 - autism1 - american psychiatric association3 - dopamine-producing nerve cells1 - myxoedema1 - thc1 - alzheimers gene1 - tuberculosis1 - a-beta protein1 -