Researchers discover how to target and disable ‘bad apple’ proteins

Yu Tian Wang
Yu Tian Wang

A new technique that targets proteins that cause disease and destroys “bad apples” in the cell has been developed by researchers at the University of British Columbia’s Brain Research Centre, part of Vancouver Coastal Health Research Institute.

The findings, published this month in Nature Neuroscience, has important implications for a variety of diseases, including Alzheimer’s, Huntington’s, stroke and even cancers, the researchers say.

“This technique is revolutionary, because it can reduce or remove the pathological form of the protein without impacting the normal form of the protein or harming other proteins in the cell,” says Xulai (Shelly) Fan, a UBC PhD candidate who co-led the study with Prof. Yu Tian Wang of UBC’s Faculty of Medicine.

The researchers used the new technique to disable protein function temporarily in select brain regions affected by disease. Directly targeting specific proteins in a cell is important, because many disease-causing proteins have normal functions in the cell. They become harmful – or bad apples – only during certain disease processes.

In a stroke, for example, the body activates a protein, DAPK1, which damages or kills neurons in the affected brain area. However, in its normal form and outside the affected brain area, DAPK1 has a positive function – clearing the body of cell mutations and inhibiting the abnormal cell growth found in cancer. Targeting is critical because permanently disabling DAPK1 outside of the affected brain area could have many adverse effects.

“If we can target these proteins temporarily we may be able to save neurons without impacting the patient’s overall health,” says Dr. Wang, who is a professor of Neurology and The Heart and Stroke Foundation of BC & Yukon Chair in Stroke Research. “This technique has broad applications, so it’s a very exciting finding.”

Source of text: UBC News

Original Research Article: Fan X, Jin WY, Lu J, Wang J, Wang YT. Rapid and reversible knockdown of endogenous proteins by peptide-directed lysosomal degradation. Nat Neurosci. 2014 Mar;17(3):471-80. doi: 10.1038/nn.3637. Epub 2014 Jan 26. – http://www.nature.com/neuro/journal/v17/n3/full/nn.3637.html

Also read a blog post by the first author of this paper, Shelly Fan, here: http://sciencewriters.ca/2014/02/19/custom-targeting-beacons-harness-cellular-executioners-to-fight-disease/