Degrading viral RNA to treat SARS-CoV-2 infection

Development of vaccines against SARS-CoV-2 has been rapid, but the rise of variants forces scientists to frequently modify treatments. Ideally, therapies would target mutation-resistant viral proteins, but this has proven difficult. Researchers reporting in ACS Central Science, however, have now developed a system that directly targets and degrades the viral RNA genome, reducing infection in mice. The method could be adapted to fight off many viruses, as well as treat various diseases.

Vaccines and antiviral drugs typically target proteins critical to viral infection and replication. This targeting induces evolutionary pressure for the virus to mutate, however, reducing the effectiveness of existing treatments and requiring development of new vaccines and drugs. To get around this issue, researchers have turned to targeting highly conserved structures within the viral RNA genome. Other groups have linked small molecule RNA binders to ribonuclease L ligands (RIBOTACs), creating degraders that relied on ribonuclease expression within cells, which varied across tissues. Avoiding this dependency, Gonçalo J. L. Bernardes, Konstantinos Tzelepis, Sigitas Mikutis and colleagues showed that attaching imidazole to RNA could degrade the nucleic acid, so they wondered whether attaching imidazole to an RNA-binding molecule would result in targeted degradation.

To accomplish this, the team used pyridostatin (PDS), which binds to G-quadruplex (G4) RNA structures, and MTDB, which binds to betacoronaviral pseudoknots, as the RNA-binding molecules. The researchers then appended each compound with a flexible linker and imidazole and called these molecules proximity-induced nucleic acid degraders (PINADs). By bringing imidazole into close proximity to the RNA, both PINADs degraded SARS-CoV-2 RNA. In addition, the compounds were effective when tested in cells infected with SARS-CoV-2 and its alpha and delta variants. Importantly, when the researchers gave the MTDB degrader to mice infected with SARS-CoV-2, viral load was reduced, as were levels of a biomarker of viral infection and replication. The researchers say that their system should allow any RNA-binding small molecule to be converted to a PINAD, so that it could someday be used to target and destroy other disease-related RNAs. This list could include disorders such as Alzheimer’s disease or Huntington’s disease, targeting the mRNAs of misfolded proteins that have otherwise proven difficult to target.

The authors acknowledge funding from the UK Research and Innovation (UKRI), the Wellcome Trust, the Jardine Foundation, the Cambridge Trust, the Agencia Estatal de Investigación, the UKRI Medical Research Council, Leukemia UK and Cancer Research UK.

The paper’s abstract will be available on April 26 at 8 a.m. Eastern time here: http://pubs.acs.org/doi/abs/10.1021/acscentsci.3c00015

The American Chemical Society (ACS) is a nonprofit organization chartered by the U.S. Congress. ACS’ mission is to advance the broader chemistry enterprise and its practitioners for the benefit of Earth and all its people. The Society is a global leader in promoting excellence in science education and providing access to chemistry-related information and research through its multiple research solutions, peer-reviewed journals, scientific conferences, eBooks and weekly news periodical Chemical & Engineering News. ACS journals are among the most cited, most trusted and most read within the scientific literature; however, ACS itself does not conduct chemical research. As a leader in scientific information solutions, its CAS division partners with global innovators to accelerate breakthroughs by curating, connecting and analyzing the world’s scientific knowledge. ACS’ main offices are in Washington, D.C., and Columbus, Ohio.

To automatically receive news releases from the American Chemical Society, contact newsroom@acs.org.

Follow us: Twitter | Facebook | LinkedIn | Instagram