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Biology subjects

Egelman, E. H.

Publications and source records attributed to Egelman, E. H..

2 recordsLinked to original sources

Cryo-EM Map of the CFA/I Pilus Rod

Enterotoxigenic Escherichia coli (ETEC) are common agents of diarrhea for travelers and a major cause of mortality in children in developing countries. To attach to intestinal cells ETEC express colonization factors, among them CFA/I, which are the most prevalent factors and are the archetypical representative of Class 5 pili. Due to their helical quaternary structure that can be unwound and works as a damper of force, CFA/I pili help ETEC bacteria withstand intestinal fluid motion. We report in this work the CFA/I pilus structure at 4.0 [A] resolution and report details of the donor strand complementation. The density map allows us to identify the buried surface area between subunits, and these regions are correlated to quaternary structural stability in class 5 and Chaperone-Usher pili. In addition, from the EM map we also predicted that residue 13 (proline) of the N-terminal {beta}-strand could have a major impact on the filaments structural stability. Therefore, we used optical tweezers to measure and compare the stability of the quaternary structure of wild type CFA/I and point-mutated CFA/I in which proline 13 was changed to a non-polar residue, phenylalanine. We found that pili with this mutated CFA/I require a lower force to unwind, supporting our hypothesis that Pro 13 is important for structural stability. The high-resolution CFA/I pilus structure presented in this work and the analysis of structural stability will be useful for the development of novel antimicrobial drugs that target the pilus structure to reduce its damping properties, which are needed for initial attachment and sustained adhesion of ETEC.\n\nSynopsisThe structure of a common virulence factor expressed on the surface of diarrheacausing bacteria, CFA/I pili, has been determined at 4.0 [A] resolution. The role of proline 13 in stabilizing the pilus structure has been confirmed using force-measuring optical tweezers on wild type and point-mutated pili.

molecular biology

The AAA+ ATPase TorsinA polymerizes into hollow tubes with a helical periodicity of 8.5 subunits per turn

TorsinA is an ER-resident AAA+ ATPase, whose single residue deletion of glutamate E303 results in the genetic neuromuscular disease primary dystonia. TorsinA is a highly unusual AAA+ ATPase in that it needs an external activator. Also, it appears not to thread a peptide substrate through a narrow central channel, in contrast to its closest structural homologs. Here, we examined the oligomerization of TorsinA to get closer to a molecular understanding of the still enigmatic function of it. We observe TorsinA to form helical filaments, which we analyzed by cryo-electron microscopy using helical reconstruction. The 4.4 [A] structure reveals long hollow tubes with a helical periodicity of 8.5 subunits per turn, and an inner cavity of [~]4 nm diameter. We further show that the protein is able to induce tubulation of membranes in vitro, an observation that may reflect an entirely new characteristic of AAA+ ATPases. We discuss the implications of these observations for TorsinA function.

biochemistry