Proteins produced in cells often undergo modifications by enzymes after they are formed. One type of modification, called prenylation, adds ‘tags’ to proteins that tells them where to go in the cell and how to interact with other proteins. However, when prenylation goes wrong, it can lead to diseases including cancer, retinal and cardiovascular diseases, and viral infections.
Because of their role in these diseases, the enzymes that cause prenylation have been targeted by potential new drugs. For example, recent work led by Dr Beata Wojciak-Stothard from the Department of Medicine at Imperial has suggested that prenylation may be an important drug target in pulmonary arterial hypertension.
However, because the mechanisms of prenylation are difficult to study, none of the potential drugs targeting it directly have so far been approved for medical use, although indirect targeting using bisphosphonate drugs is an important treatment for osteoporosis.
Now, researchers led by Professor Ed Tate, from the Department of Chemistry at Imperial, have developed a new way to track prenylation that does not affect the normal working of a cell, allowing them to profile the full range of prenylation inside the cell.
Professor Tate said: “All previous studies used drugs called statins to suppress prenylation and favor incorporation of chemical tags, but statins have widespread impacts on cells, making those experiments very difficult to interpret. We developed tags that not only work without statins, but can also analyze different prenylation pathways in parallel, which has not been possible before.
“This also allows us to understand the interplay between the different pathways for the first time, as well as to get a lot more information about each individually since all our analytical power can be focused on one at a time.”
The recent study, published in Nature Chemistry, describes two new chemical tags that can be used to detect protein prenylation inside living cells without any need for disruption of a normal cellular environment. The new tags match closely the natural prenylation tags found in cells and are therefore used just as readily by the prenylating enzymes.
For the first time the researchers were able to detect the full range of proteins that are prenylated in cells in a single experiment and to discover new proteins that where not previously known to be prenylated.
They were also able to observe switching between prenylation pathways in response to treatment with anticancer drugs, providing the first global insights into this process, which is important for drug resistance.
