Researchers from the Technion and the University of Tokyo have identified unique peptides with potential anti-cancer properties.
A study recently published in Nature Communications highlights the potential of unique peptides as anti-cancer agents. Peptides, which are short chains of amino acids connected by peptide bonds, have garnered attention for their potential role in cancer treatment.
Unlike proteins that usually contain hundreds of amino acids, peptides contain – at most – dozens of such acids. The cyclic peptides the researchers discovered bind specifically to chains of ubiquitin proteins – proteins that are usually used as a “death tag” for damaged proteins. The labeling of the damaged proteins leads to their being broken down in the proteasome, or the cell’s “garbage can.”
Peptides typically contain no more than a few dozen amino acids, in contrast to proteins which usually contain hundreds. The cyclic peptides recently discovered by researchers have the ability to bind specifically to chains of ubiquitin proteins, which are often used as a “death tag” for damaged proteins. These marked proteins are then broken down in the proteasome, a cellular structure responsible for removing waste.
The research was conducted by Professor Ashraf Brik, Dr. Ganga B. Vamisetti, and Dr. Abbishek Saha from the Schulich Faculty of Chemistry at the Technion – Israel Institute of Technology, along with Professor Nabieh Ayoub from the Technion’s Faculty of Biology and Professor Hiroaki Suga from the University of Tokyo.
The discovery of the ubiquitin system led to the awarding of the 2004 Nobel Prize in Chemistry to three researchers, including Distinguished Professors Aharon Ciechanover and Avraham Hershko of the Technion’s Ruth and Bruce Rappaport Faculty of Medicine.
Targeting Ubiquitin Chains for Cancer Therapy
Over the years, it became clear that the activity of the ubiquitin system depends in part on the point where the ubiquitin molecules are linked to each other in the chain. For example, linking the ubiquitin in the chain at position 48 (K48) leads to the removal of proteins to the proteasome, while linking the ubiquitin at position 63 (K63) leads to the repair of damaged DNA.
In recent years, Technion researchers have developed a new approach to influencing the ubiquitin mechanisms. Instead of interfering with the activity of enzymes that affect these mechanisms, they decided to try to directly intervene in the ubiquitin chain itself.
Based on this approach, the researchers in a previous work developed cyclic peptides that bind the K48-linked ubiquitin chains, preventing them from leading to the breakdown of the damaged proteins. This disruption gradually leads to the programmed death of cells. In the same study, they hypothesized and then proved that when such an event formed in a malignant tumor, it kills the cancer cells, potentially protecting the patient. This discovery, published in 2019 in the journal Nature Chemistry, led to the establishment of a new startup that is advancing the discovery toward clinical use.
In the current study, cyclic peptides that bind the chains linked to position 63 in ubiquitin and that are involved in repairing damaged DNA were discovered. The researchers found that when attached to these ubiquitin chains, such peptides disrupt the aforementioned repair mechanism. This leads to the accumulation of damaged DNA, and to cell death. Here too, when this binding occurs in cancer cells, it destroys these cells. The researchers believe this therapeutic strategy could be more effective than existing anti-cancer drugs, against which patients gradually develop resistance.
References:
“Selective macrocyclic peptide modulators of Lys63-linked ubiquitin chains disrupt DNA damage repair” by Ganga B. Vamisetti, Abhishek Saha, Yichao J. Huang, Rajeshwer Vanjari, Guy Mann, Julia Gutbrod, Nabieh Ayoub, Hiroaki Suga and Ashraf Brik, 18 October 2022, Nature Communications.
DOI: 10.1038/s41467-022-33808-6
“De novo macrocyclic peptides that specifically modulate Lys48-linked ubiquitin chains” by Mickal Nawatha, Joseph M. Rogers, Steven M. Bonn, Ido Livneh, Betsegaw Lemma, Sachitanand M. Mali, Ganga B. Vamisetti, Hao Sun, Beatrice Bercovich, Yichao Huang, Aaron Ciechanover, David Fushman, Hiroaki Suga and Ashraf Brik, 10 June 2019, Nature Chemistry.
DOI: 10.1038/s41557-019-0278-x
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