Overview

The Markus Seeliger Lab is actively seeking enthusiastic graduate students and post-doctoral researchers to join our team.

 

We’re committed to building a positive and productive lab environment that supports the professional goals of all our members. Our lab is productive, within the last year we have published or have had accepted 8 papers in well-regarded journals (PNAS, JMB, JBC, Mol Cell Oncology, Angewandte, Nat Chem Bio, Nat Comm, Biomolecules). Our group also maintains active research collaborations with labs at Stony Brook, in NYC, across the United States, and even internationally. For example, three of our graduate students recently travelled to Frankfurt, Germany (May 2022).

Interested graduate students or candidates for postdoctoral positions should contact Markus at markus.seeliger@stonybrook.edu.

Our research group is interested in the molecular mechanism that underlies the signaling of protein tyrosine kinases and ubiquitin ligases. Protein kinases are well established drug targets in oncology and inflammatory diseases. Kinases can access multiple well defined structural states and we are studying how small molecule inhibitors interact with these structures.

The aim for these NIH funded projects is to understand the conformational exchange between kinase conformations as well as to understand the inhibitory mechanism of kinase inhibitors. For this we are using X-ray crystallography, nuclear magnetic resonance spectroscopy (NMR), protein engineering and other biophysical methods in collaboration with computational biologists. The ubiquitin system relies on a highly modular system of enzymes to ligate ubiquitin onto substrate proteins which in many cases leads to the degradation of the substrate protein via the proteasome. The potential of the ubiquitin system as a therapeutic target is illustrated by the success of the proteasome inhibitor bortezomib in the treatment of multiple myeloma. We are interested in applying concepts from the field of protein kinase research to the study of ubiquitin conjugating enzymes (E2) and ubiquitin ligases (E3) with the aim of enabling specific therapeutics. Our current aim is to study the change in substrate spectra of ubiquitin ligases upon aging in yeast cells. This is work is generously supported by the Ellison Medical Foundation.