Benjamin Glick

Sr. Fellow,
- Professor, Dept. of Molecular Genetics & Cell Biology and Institute for Biophysical Dynamics, University of Chicago

Contact Information

Department of Molecular Genetics & Cell Biology
The University of Chicago
920 E. 58th St., CLSC 829A
Chicago, IL 60637

Phone: 773 702 5315
Fax: 773 702 5315
Email: .(JavaScript must be enabled to view this email address)


Our main goal is to understand the processes that generate Golgi stacks. The cisternal maturation model provides a conceptual framework for studying Golgi formation. This model postulates that new Golgi elements arise at transitional ER (tER) sites, which are specialized for the production of ER-to-Golgi transport vesicles. We have obtained evidence that in budding yeasts, Golgi distribution is a consequence of tER organization. In Saccharomyces cerevisiae, Golgi cisternae are dispersed throughout the cytoplasm and the entire ER network functions as tER, whereas in Pichia pastoris, ordered Golgi stacks are located next to discrete tER sites. We are analyzing these two yeasts in parallel with vertebrate cells. Our specific approaches are: (1) To characterize the inheritance and dynamics of Golgi cisternae in S. cerevisiae through a combination of genetics and 4D video microscopy. (2) To study tER organization and biogenesis in P. pastoris using genetics, molecular biology, video microscopy, and biophysical computer simulations. P. pastoris is an ideal model organism for these studies. (3) To explore tER organization and dynamics in vertebrate cells. This approach is revealing evolutionarily conserved mechanisms that generate tER sites.

A second project in the lab involves optimizing the red fluorescent protein DsRed. Like GFP, DsRed potentially has wide application as a reporter and fusion tag. However, wild-type DsRed matures very slowly, requiring more than 24 hours at 37 C to achieve maximal fluorescence. We overcame this problem by using directed evolution to create rapidly maturing DsRed variants, one of which is now marketed commercially as DsRed-Express. Wild-type DsRed also tetramerizes, limiting its usefulness as a fusion tag. Ongoing work is aimed at creating a monomeric DsRed variant that will be as versatile as GFP.

Research Papers