Samagya Banskota

Using viruslike particles to deliver therapies safely and effectively

Stylized illustration portrait of Samagya Banskota by Jessine Hein.

Jessine Hein

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Samagya Banskota grew up in a family of doctors in Nepal, aware from a young age of how physicians could change people’s lives. Today she is a biomedical engineer at Boston University, studying ways to create safer, more effective therapies for a multitude of diseases.

Banskota is creating so-called viruslike particles to deliver gene-editing technologies to cells. These engineered particles have protein structures that resemble those of viruses and can target specific cells in the body, but they lack any genetic material of their own, so they’re not infectious. By packaging gene-editing tools in this way, her team has been able to avoid the problems associated with using actual viruses to deliver therapies.


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Portrait photograph of Samagya Banskota by Tony Luong.

Tony Luong

Other investigators have shown that viruslike particles can deliver gene-editing machinery to cells in petri dishes. But Banskota and her colleagues were the first to successfully demonstrate this approach in living organisms at a therapeutic level, restoring partial visual function in mice with genetic blindness. “Proteins have the shortest half-life, so they go in, they do the job, and they just get destroyed within a few hours,” she explains. “We don’t have to worry about any other side effects that may come from prolonged expressions of these systems.”

These viruslike particles could be used to deliver therapies other than gene-editing materials, Banskota notes. Antibody drugs such as Herceptin, for breast cancer, are lab-engineered proteins. They can be very powerful, but they work by targeting proteins on the outside of cells. The drivers of a lot of human diseases—including several cancers and neurological diseases—are located inside cells, where such therapies can’t reach them. “With our delivery system being so good for protein delivery,” Banskota says, “I think it opens up a whole new category of medicines for diseases that we potentially can treat.”

This article is part of The Young American Scientists, an editorially independent project that was produced with financial support from Regeneron.

Kate Wong is an award-winning science writer and senior editor for features at Scientific American, where she has focused on evolution, ecology, anthropology, archaeology, paleontology and animal behavior. She is fascinated by human origins, which she has covered for nearly 30 years. Recently she has become obsessed with birds. Her reporting has taken her to caves in France and Croatia that Neandertals once called home to the shores of Kenya’s Lake Turkana in search of the oldest stone tools in the world, as well as to Madagascar on an expedition to unearth ancient mammals and dinosaurs, the icy waters of Antarctica, where humpback whales feast on krill, and a “Big Day” race around the state of Connecticut to find as many bird species as possible in 24 hours. Wong is co-author, with Donald Johanson, of Lucy’s Legacy: The Quest for Human Origins. She holds a bachelor of science degree in biological anthropology and zoology from the University of Michigan. Follow her on Bluesky @katewong.bsky.social

More by Kate Wong
Scientific American Magazine Vol 335 Issue 1This article was published with the title “Samagya Banskota” in Scientific American Magazine Vol. 335 No. 1 (), p. 36
doi:10.1038/scientificamerican072026-5ofVAylBjRneEmDRqYeq1v

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