What I do
I research and teach biochemistry, and often try to fuse those two pursuits.
structural biology, biochemistry, biophysics, and bacterial genetics<br>science education<br>
- Ph.D., Biophysics, University of Michigan, 2013
- MA, Chemistry, Wesleyan University, 2008
- BA, Molecular Biology & Biochemistry, Wesleyan University, 2007
It has long been known that nucleic acids carry the genetic information necessary for life. Nucleic acids also play vital structural, catalytic, and regulatory roles in the cell. Very recently, we discovered that nucleic acids perform an additional unsuspected but crucial task—preventing protein aggregation as molecular chaperones. We showed that nucleic acids possess very potent anti-aggregation activity. By weight, RNA is at least an order of magnitude more abundant in the cell than known chaperone proteins, and in vitro, we found that RNA is 5- to 300-fold more effective at preventing protein aggregation. Moreover, we showed that RNA can work with cellular protein folding machinery to refold denatured proteins. These findings raised the possibility that RNA plays a sizable and possibly dominant role in protein stability in the cell. Currently, we know virtually nothing of the principles by which nucleic acids with chaperone activity function, the extent of their abilities, or of the mechanism by which they interact and cooperate with other protein chaperones. Knowledge of how nucleic acids affect protein aggregation will provide crucial insights into the alternative mechanisms that cells developed to prevent toxic aggregation and disease. The work in the Horowitz lab is focused on understanding this phenomenon.
- Investigating the Chaperone Activity of Nucleic Acids