Kristen Naegle

Naegle, Kristen

Primary Appointment

Biomedical Engineering

Education

  • BS, Electrical Engineering, University of Washington
  • MS, Electrical Engineering, University of Washington
  • MS, Biological Engineering, Massachusetts Institute of Technology
  • PhD, Biological Engineering, Massachusetts Institute of Technology

Contact Information

409 Lane Road
MR4 1116
Charlottesville, MO 22903
Email: kmn4mj@virginia.edu

Research Disciplines

Biochemistry, Bioinformatics and Genomics, Biotechnology, Cancer Biology, Cell and Developmental Biology, Computational Biology, Experimental Pathology, Molecular Biology, Structural Biology

Research Interests

Regulation and function of tyrosine phosphorylation in complex networks

Research Description

Tyrosine phosphorylation is a protein modification that can occur during or after translation of a protein.The phosphate addition to a tyrosine residue, regulated by tyrosine kinases and phosphatases, can result in changes in protein function, regulation and localization. It is key to important cell signaling processes, which are the processes that convert extracellular cues, like growth factors and insulin, into biochemical networks that result in a change to the cell. Tyrosine phosphorylation is specifically utilized in the early events of receptor tyrosine kinase (RTK) networks, which are fundamental to many processes in the development and homeostasis of complex organisms. Improvements in measurement technologies have enabled the ability to detect and monitor tyrosine phosphorylation and now we know that tyrosine phosphorylation is extensive — occurring on thousands of tyrosines in the human proteome.

Given the sheer size of the challenge, we use both computational and molecular technologies to predict and test the role of tyrosine phosphorylation on proteins and in cellular networks. Although we incorporate new mathematical and computational methods as needed to tackle the fundamental problems of our research, those techniques always have a foundation in statistical robustness. Hypotheses are tested in molecular and cellular systems, closing the loop between computation and experimentation.

The questions that drive us include:


  • How do we increase the capabilities of research to gain new understanding of tyrosine phosphorylation rapidly, i.e. in a high-throughput manner that matches the rate of discovery of these modifications?

  • How do we develop new capabilities to understand how these networks act in specific contexts? Cell context refers to the differences we see between tissue types and the states of the network components that lead to differential responses of tissues to the same cue. As a philosophy, we approach network dysregulation that occurs in disease as an alteration in cell context.

Selected Publications