نتایج جستجو برای: pore forming toxin

تعداد نتایج: 200158  

Journal: :Journal of innate immunity 2014
Russell E N Becker Bryan J Berube Georgia R Sampedro Andrea C DeDent Juliane Bubeck Wardenburg

Immunomodulatory cytotoxins are prominent virulence factors produced by Staphylococcus aureus, a leading cause of bacterial sepsis, skin infection, and pneumonia. S. aureus α-toxin is a pore-forming toxin that utilizes a widely expressed receptor, ADAM10, to injure the host epithelium, endothelium, and immune cells. As each host tissue is characterized by a unique composition of resident cells ...

2017
Emeline Reboud Pauline Basso Antoine P. Maillard Philippe Huber Ina Attrée

Bacterial toxins are important weapons of toxicogenic pathogens. Depending on their origin, structure and targets, they show diverse mechanisms of action and effects on eukaryotic cells. Exolysin is a secreted 170 kDa pore-forming toxin employed by clonal outliers of Pseudomonas aeruginosa providing to some strains a hyper-virulent behaviour. This group of strains lacks the major virulence fact...

2013
Sabrina Hupp Christina Förtsch Carolin Wippel Jiangtao Ma Timothy J. Mitchell Asparouh I. Iliev

The eukaryotic actin cytoskeleton is an evolutionarily well-established pathogen target, as a large number of bacterial factors disturb its dynamics to alter the function of the host cells. These pathogenic factors modulate or mimic actin effector proteins or they modify actin directly, leading to an imbalance of the precisely regulated actin turnover. Here, we show that the pore-forming, chole...

1998
EHUD GAZIT PAOLO LA ROCCA MARK S. P. SANSOM YECHIEL SHAI

The aim of this study was to elucidate the mechanism of membrane insertion and the structural organization of pores formed by Bacillus thuringiensis d-endotoxin. We determined the relative affinities for membranes of peptides corresponding to the seven helices that compose the toxin pore-forming domain, their modes of membrane interaction, their structures within membranes, and their orientatio...

Journal: :Biophysical journal 2011
James R Thompson Bríd Cronin Hagan Bayley Mark I Wallace

We have observed the assembly of the staphylococcal pore-forming toxin α-hemolysin using single-molecule fluorescence imaging. Surprisingly, assembly from the monomer to the complete heptamer is extremely rapid, occurring in <5 ms. No lower order oligomeric intermediates are detected. Monte Carlo simulation of our experiment shows that assembly is diffusion limited, and pore formation is depend...

Journal: :Cell 2005
Sarah J. Tilley Elena V. Orlova Robert J.C. Gilbert Peter W. Andrew Helen R. Saibil

The bacterial toxin pneumolysin is released as a soluble monomer that kills target cells by assembling into large oligomeric rings and forming pores in cholesterol-containing membranes. Using cryo-EM and image processing, we have determined the structures of membrane-surface bound (prepore) and inserted-pore oligomer forms, providing a direct observation of the conformational transition into th...

Journal: :Microbial pathogenesis 2008
Mary E Hensler Darin Quach Chia-Jun Hsieh Kelly S Doran Victor Nizet

The Gram-positive pathogen Group B Streptococcus (GBS) is the leading cause of bacterial pneumonia, sepsis, and meningitis in human newborns. GBS elaborates a pore-forming toxin known as CAMP factor that synergizes with Staphylococcus aureus beta-toxin, generating a co-hemolytic reaction useful in identification of GBS in the clinical laboratory. To evaluate the indirect evidence implicating CA...

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