Specific complexes of protein and RNA carry out many essential biological functions, including RNA processing, RNA turnover, RNA folding, as well as the translation of genetic information from mRNA into protein sequences. Our group is interested in studying RNA-protein interactions and translational control of gene expression. We are also interested in understanding how sequence and structure in RNA-binding proteins contribute to the formation of RNA-protein complexes and promote specific biological functions. We use a combination of molecular genetics, protein biochemistry, and structural approaches to determine the biological function and mechanism of action of specific RNA-protein complexes. A major research focus in our group concerns the SmpB•SsrA quality control system for protein tagging, directed degradation, and ribosome rescue. Current emphasis is on molecular characterization of how the SmpB protein recognizes SsrA RNA and promotes the detection and rescue of stalled ribosomes. The relative simplicity of the SmpB-SsrA interaction, the stability of the complex, and recruitment of additional novel factors during trans-translation makes this an ideal system for studying the basic principles that govern the assembly of RNA-protein complexes.

Insights gained from these investigations should further illuminate the scope of a fundamental process of life, translation. More significantly, a thorough understanding of this unique bacterial system, essential for survival of many pathogenic bacteria, should pave the way for the development of novel knowledge-based anti-infective agents that exclusively target pathogenic microorganisms. Ultimately, these insights should have implications for a better understanding of a variety of cellular processes, including the replication of RNA viruses, control of gene expression, and the synthesis and degradation of proteins.