We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.


New Protein Identification Method May Support Drug Discovery

Protein structure.
The illustration shows how different areas of PRC2 protein (the one on the right side) binds to survivin. The researchers chopped the PRC2 sequence into units of 15 amino acids and arranged them on a grid. Each pixel in that grid is 1 unit. The colour shows binding strength to survivin. Blue means the unit in that pixel doesn't bind/binds weakly to survivin, and the bright pink pixels are the strongest binders. Credit: Atsarina Larasati Anindya.
Listen with
Register for free to listen to this article
Thank you. Listen to this article using the player above.

Want to listen to this article for FREE?

Complete the form below to unlock access to ALL audio articles.

Read time: 2 minutes

All living cells contains proteins with different functions, depending on the type of cell. Researchers at the University of Gothenburg have discovered a way to identify proteins even without looking at their structure. Their method is faster, easier and more reliable than previous methods.

Currently, the general view is that each protein’s structure is what controls its function in cells. The atomic sequences, meaning how the atoms are arranged in the proteins, create the protein’s structure and shape. But there are many proteins that lack a well-defined structure.

Researcher Gergely Katona has developed a new method where proteins are scanned based on the number of amino acids (or the number of different atoms) they contain in order to identify them and their function instead of identifying them based on their structure. With this scanning method, the researchers were able to predict relatively reliably which combination of amino acids is needed to bind to the protein survivin. The outcome was a reliability of about 80 per cent, which is better than when you use the protein’s primary structures for identification. The results are now published in the scientific journal iScience.

Want more breaking news?

Subscribe to Technology Networks’ daily newsletter, delivering breaking science news straight to your inbox every day.

Subscribe for FREE

The structure of less importance

Several thousand peptides containing 15 amino acids were tested and the researchers were able to conclude that it was the amino acid content that affected their binding to survivin, while the structure of the peptides had almost no significance.

“Simple counting things has often been a successful method in science. Here we counted the number of amino acids and were able to predict the function of the protein surprisingly well,” says Gergely Katona.

The researchers see advantages with this method of scanning proteins. Machine learning (AI) also speeds up the process of linking the number and type of amino acids to a certain function. This in turn means that the development of new biological drugs can be accelerated.

In the researchers’ experiments with this new scanning method, a completely new function of the protein survivin was also discovered. This protein is mainly prominent in embryo cells and prevents programmed cell death. But in cancerous tumours, survivin becomes unregulated and thus facilitates the development of the cancer.

Useful in cancer research

The researchers have now seen that survivin directly influences another protein, PRC2, which switches off and on various functions in the DNA in the cell, like a kind of programming. Dysfunctional PRC2 can also be linked to various forms of cancer. Today’s cancer drugs target both survivin and PRC2, but with the newly discovered link between survivin and PRC2, the drugs may need to be designed differently to avoid serious side effects.

“We saw that if we suppressed the level of survivin, activity in PRC2 increased. The dream for pharmaceutical companies is to find the right targets in the atomic sequences to be able to balance the two proteins,” says Gergely Katona.

Reference: Jensen M, Chandrasekaran V, García-Bonete MJ, et al. Survivin prevents the polycomb repressor complex 2 from methylating histone 3 lysine 27. iScience. 2023;26(7):106976. doi: 10.1016/j.isci.2023.106976

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.