Biological Sciences prof compares normal and abnormal genes to shed light on Lou Gehrig’s disease
by Chris Jarvis
“I had always been amazed at how everything is able to work inside the cell,” said Galaleldeen, who is now an Assistant Professor of Biological Sciences at St. Mary’s. “But to realize you could contribute to public knowledge in this way — it was fascinating.”
Think of it as Galaleldeen’s “aha moment.”
To structural biologists like Galaleldeen, molecular diagrams are blueprints for molecular structures including proteins, which are an integral part of all living things. These diagrams can be treasure troves of medical information, giving clues for new drug therapies and vaccinations.
Galaleldeen’s current research focuses on outlining mutations in the gene superoxide dismutase 1 (SOD1), an essential enzyme for normal cell activity. Abnormalities in SOD1 have been linked to Lou Gehrig’s disease, or ALS (amyotrophic lateral sclerosis, which attacks the cells that control muscles), and Galaleldeen hopes that comparing normal and abnormal gene structures might give insight into the origins of ALS or even an effective treatment.
“People have been working on ALS for 160 years now, since it was discovered, but we do not have a single drug that can make a person live one month longer,” Galaleldeen said.
Though ALS remains a mystery, work like Galaleldeen’s to understand its molecular makeup is a significant piece of the puzzle. In June 2013, Galaleldeen was named a Biaggini Research Program fellow at St. Mary’s, allowing him to continue his research.
Outlining molecular structures is a tedious process, but one Galaleldeen pursues with verve.
“It’s exciting that you might get to figure out something nobody else will, especially when you have a hot project and you’re competing with other scientists,” he said. “It’s not sports, but it is a competition for the brain.”