Maryan Raeeszadeh-Sarmazdeh: Engineering stimuli-responsive therapeutics for developing novel therapeutics and drug delivery tools
Engineering stimuli-responsive therapeutics for developing novel therapeutics and drug delivery tools
Chemical and Materials Engineering
Maryam Raeeszadeh-Sarmazdeh, Ph.D. joined the University of Nevada, Reno in July 2019 as an assistant professor. Maryam was a senior research fellow in the Department of Cancer Biology at Mayo Clinic, Florida, during which her work was focused on engineering novel protein-based therapeutics based on natural enzyme inhibitors. Prior to her appointment at Mayo Clinic, she was a postdoctoral scholar at the Chemical and Biomolecular Engineering Department at the University of Delaware. Her research at University of Delaware was focused on enzyme and metabolic pathway engineering for generating biofuel. Maryam earned her Ph.D. in chemical and biomolecular engineering from the University of Tennessee at Knoxville. There, her research was focused on generating site-specific protein immobilization on the surface and protein engineering using yeast surface display and directed evolution.
The Sarmazdeh Lab is at the interface of life science and engineering. Our group has a dynamic and diverse environment and welcomes bright and motivated students from different backgrounds interested in protein engineering and design. One of our recent undergraduate researches won the UROP-INBRE award. Students with knowledge and interest in bioengineering, protein biochemistry and molecular biology are encouraged to apply. More information can be found on the Sarmazdeh lab website. For the latest news follow our twitter: @sarmazdehlab.
One of the main issues with cancer therapeutics are the side effects which sometimes are worse than the disease itself. To overcome the undesired effects of drugs, we need to design a smart stimuli-responsive system which gets triggered at the tumor site. This site-specific activation and delivery. This project involves design and engineering protein switches which respond to external stimuli at the tumor site.