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Unlocking RNA functionality: A redox-responsive approach

Date:
June 6, 2024
Source:
National University of Singapore
Summary:
Chemists have developed a strategy using disulfide-containing small molecules to facilitate the reversible control and delivery of ribonucleic acid (RNA). A research team has developed a method that takes advantage of a chemical process called post-synthetic RNA acylation chemistry, and combined it with dynamic disulfide exchange reaction for RNA delivery and reversible control. This method provides a way to mask the RNA molecule, and researchers can potentially regulate its activity and delivery until it reaches its target site within the cell.
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National University of Singapore (NUS) chemists have developed a strategy using disulfide-containing small molecules to facilitate the reversible control and delivery of ribonucleic acid (RNA).

RNA-based therapeutics have emerged as one of the most sought-after therapeutic modalities in recent years. However, RNA delivery remains a major challenge in the field. Lipid nanoparticles, despite being widely used for RNA delivery including the delivery of Covid-19 mRNA vaccines, face several limitations such as their effectiveness and safety. Alternative methods that can potentially overcome these limitations are highly desirable.

A research team led by Assistant Professor ZHU Ru-Yi from the NUS Department of Chemistry have developed a method that takes advantage of a chemical process called post-synthetic RNA acylation chemistry, and combined it with dynamic disulfide exchange reaction for RNA delivery and reversible control. This method provides a way to mask the RNA molecule, and researchers can potentially regulate its activity and delivery until it reaches its target site within the cell.

The research findings were published in the journal Angewandte Chemie International Edition on 13 March 2024.

The researchers found that by adding special chemical markers comprising disulfide-containing groups to the RNA, these groups can block RNA's catalytic activity and folding, temporarily hiding the instructions. Then, when needed, they can activate the RNA by removing these markers, allowing cells to read and act upon the instructions again. This strategy allows the RNA to enter cells quickly, distribute effectively, and become active in the cell's cytosol without getting trapped in lysosomes. The researchers believe that their methodology will be accessible to laboratories engaged in RNA biology and holds promise as a versatile platform for RNA-based applications.

Asst Prof Zhu said, "Our studies showcase the first example of RNA delivery into cells using only small molecules."

"The simplicity of our method for modifying RNA and the unique delivery mechanism will undoubtedly attract more researchers to adopt and improve the method. We believe that our work will facilitate numerous applications in the field of RNA biology and biomedicines," added Asst Prof Zhu.

Looking ahead, the research team is actively designing new strategies to modify RNA and improve RNA-based therapeutics.


Story Source:

Materials provided by National University of Singapore. Note: Content may be edited for style and length.


Journal Reference:

  1. Junsong Guo, Siqin Chen, Yoshiyuki Onishi, Qi Shi, Yangyang Song, Hui Mei, Leilei Chen, Eric T. Kool, Ru‐Yi Zhu. RNA Control via Redox‐Responsive Acylation. Angewandte Chemie International Edition, 2024; 63 (21) DOI: 10.1002/anie.202402178

Cite This Page:

National University of Singapore. "Unlocking RNA functionality: A redox-responsive approach." ScienceDaily. ScienceDaily, 6 June 2024. <www.sciencedaily.com/releases/2024/06/240606152333.htm>.
National University of Singapore. (2024, June 6). Unlocking RNA functionality: A redox-responsive approach. ScienceDaily. Retrieved June 20, 2024 from www.sciencedaily.com/releases/2024/06/240606152333.htm
National University of Singapore. "Unlocking RNA functionality: A redox-responsive approach." ScienceDaily. www.sciencedaily.com/releases/2024/06/240606152333.htm (accessed June 20, 2024).

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