Award details

POTRA domain structure and function by NMR spectroscopy

Reference	BB/F000472/1
Principal Investigator / Supervisor	Professor Michael Overduin
Co-Investigators / Co-Supervisors	Professor Ian Henderson
Institution	University of Birmingham
Department	Cancer Sciences
Funding type	Research
Value (£)	375,447
Status	Completed
Type	Research Grant
Start date	01/10/2007
End date	30/09/2010
Duration	36 months

Abstract

We aim to: 1. To elucidate the three dimensional structure of the POTRA domain, characterizing its novel fold, as well as the basis for its extraordinary thermal stability. The structures of individual POTRA domains, which are repeated five times in Omp85 proteins, will be contrasted determine whether there are speciallized structural features that could mediate distinct biochemical functions. 2. To determine the POTRA domain's ligand binding properties and sites for peptide motifs responsible for recruitment of unfolded proteins for secretion. The interactions with lipid and polysaccharide components of the outer membrane will also be tested to investigate whether the POTRA domain plays a direct role in membrane attachment and insertion. Structures of complexes will be determined to identify key interactions that recognize unfolded protein substrates and membrane lipids. 3. To characterize the dynamics of the POTRA domain repeats and linkers as a function of peptide occupancy and lipid association. The mobilities of the individual residues within the POTRA domain and linkers will be contrasted in the free and bound states in order to define their effects of binding on the recruitment of proteins for secretion into the membrane.

Summary

In this research project, the three dimensional structures and biochemical functions of proteins found in the outer membrane of Gram-negative bacteria will be analyzed by spectroscopic methods. The proteins are known as autotransporters. They are responsible for the secretion of materials out of the bacterial cell and into the outer membrane and surrounding environment. Here we focus on a component of these proteins called the POTRA domain which is thought to be responsible for recruiting bacterial proteins for secretion. Gram negative bacteria are characterized by an outer membrane that surrounds a polymeric network known as peptidoglycan. The main function of the outer membrane is to form a semi-permeable layer around the peptidoglycan to protect the bacterial cell. Proteins are inserted into the outer membrane in order to control its permeability. The analysis of many bacterial genomes has revealed that POTRA domain-containing autotransporters are universally found in outer membranes of Gram negative bacteria, and are essential for their survival. In fact, this system is the most widely used protein secretion system within all Gram-negative bacteria. The POTRA domain-containing autotransporters are needed to form bacterial outer membranes and to insert proteins correctly. Some of the proteins inserted into the outer membrane of pathogenic bacteria are important antigens that act as targets of protective immune responses. Understanding how the POTRA domain recognizes and assembles these proteins is important for targeting pathogenic bacteria and for manipulating the immune response during a bacterial infection. The outer membranes of different types of Gram-negative bacteria contain a variety of lipids in addition to proteins. The outer leaflet is composed of lipopolysaccharides, glycolipids and phospholipids which differ between bacterial species. The type of lipid in the outer membrane is essential for the assembly of proteins into the membrane, and also have important roles in immune response. Consequently, we will also investigate the role of the lipids and membrane on POTRA domains, which exist next to the membrane and help to usher proteins into and through the membrane, in order to better understand how POTRA domains are oriented and active at the membrane surface.

Committee	Closed Committee - Biomolecular Sciences (BMS)
Research Topics	Structural Biology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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