Now, scientists at The Wistar Institute report new findings that further elucidate how sirtuins work and suggest how scientists might identify or design an activator to boost sirtuin activity using a structure-based approach. The research will be published Tuesday, May 18, in the Proceedings of the National Academy of Sciences.
"We know that the Sir2 sirtuin silences gene expression and stabilizes the genome in yeast," says Wistar professor Ronen Marmorstein, Ph.D., senior author of the study. "We also know that sirtuins are highly conserved in humans. The idea researchers are exploring is that if we could activate sirtuins, perhaps we could promote genomic stability and decrease cancer as well as other aging-related problems."
Marmorstein's research team has been focusing on the molecular details of how sirtuins work. Sirtuins are a family of enzymes, proteins that facilitate chemical reactions that involve converting a substrate to a product, forming intermediate substances along the way. Using a yeast sirtuin protein as a model, Marmorstein and his research team captured three-dimensional images of the sirtuin protein in association with a substrate and intermediate mimics, while in previous research his group determined the structure of the protein in association with product. Together, Marmorstein's work provides a comprehensive structural picture of enzymatic activity of sirtuins, an important step toward
Contact: Franklin Hoke
The Wistar Institute