Abstract
The human pathogen Helicobacter pylori is known for its colonization of the upper digestive system, where it escapes the harsh acidic environment by hiding in the mucus layer. One factor promoting this colonization is the helical cell shape of H. pylori. Among shape determining proteins are cytoskeletal elements like the recently discovered bactofilins. Bactofilins constitute a widespread family of polymer-forming bacterial proteins whose biology is still poorly investigated. Here we describe the first biochemical analysis of the bactofilin HP1542 of H. pylori reference strain 26695. Purified HP1542 forms sheet-like 2D crystalline assemblies, which clearly depend on a natively structured C-terminus. Polymerization properties and protein stability were investigated. Additionally, we also could demarcate HP1542 from amyloid proteins that share similarities with the bactofilin DUF domain. By using zonal centrifugation of total H. pylori cell lysates and immunfluorescence analysis we revealed peripheral membrane association of HP1542 mostly pronounced near mid-cell. Interestingly our results indicate that H. pylori bactofilin does not contribute to cell wall stability. This study might act as a starting point for biophysical studies of the H. pylori bactofilin biology as well as for the investigation of bactofilin cell physiology in this organism. Importantly, this study is the first biochemical analysis of a bactofilin in a human pathogen.
Highlights
In recent decades, bacterial cell biology has seen great advances including the discovery of novel cytoskeleton proteins exclusively found in bacteria [1]
It was previously published that the H. pylori bactofilin forms high-molecular aggregates when overexpressed in E. coli [37] in our hands HP1542 could be purified as a soluble protein under standard conditions
Our work provides the first insight into the properties of H. pylori reference strain 26695 bactofilin homolog HP1542 in terms of protein polymerization, protein stability and aggregation
Summary
Bacterial cell biology has seen great advances including the discovery of novel cytoskeleton proteins exclusively found in bacteria [1]. A recent addition to these bacteria-specific cytoskeletal proteins are the so-called bactofilins [2]. These small proteins are widespread among most bacterial lineages and involved in a variety of different cellular processes. A further characteristic of bactofilins is their ability to polymerize spontaneously in the absence of nucleotides or other cofactors [2].
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