Terje Dokland, Ph.D.
Associate Professor
Department of Microbiology

Telephone: (205) 996-4502
Office Location: BBRB 311, zip 2170
Email: dokland@uab.edu

Research Focus:  Structure and assembly of viruses

Biography | Lab Research Focus | References on PubMed

Lab Research Focus

The focus of my lab is the structure and assembly of viruses, bacteriophages and prokaryotic cells. These systems are studied with an array of structural and biophysical techniques, in particular cryo-electron microscopy (EM) and three-dimensional reconstruction, and X-ray crystallography. Among the projects that we work on are bacteriophages of Staphylococcus aureus, the porcine arterivirus PRRSV and prokaryotic cells like Bacillus anthracis, the causative agent of anthrax.

S. aureus carries genes for numerous toxins (including TSST-1, the toxic shock syndrome toxin) on so-called “pathogenicity islands” (SaPIs) in their genomes. Normally stable, these SaPIs get mobilized by infection with specific phages, allowing spread of the pathogenicity factors through the population. We are interested in this multi-step mobilization process, which includes de-repression, excision, capsid assembly and DNA packaging. This system is studied with a multi-faceted approach that includes structure determination as well as mass spectrometry and biochemical analysis.

Another project in the lab involves the structure and assembly of PRRSV, an important porcine pathogen that is a member of the Arteriviridae family of enveloped (+)RNA viruses. By combining X-ray crystallographic or NMR structures of individual proteins with overall structures obtained by electron tomography, a description of the whole virion structure can be obtained.

We also study prokaryotic ultrastructure by electron tomography of whole and cryo-sectioned cells. In particular, we are interested in structure and assembly of the B. anthracis exosporium, an important pathogenicity determinant in this system.