The GAP Portion ofPseudomonas AeruginosaType III Secreted Toxin ExoS Upregulates Total and Surface Levels of Wild Type CFTR
Author(s) -
Deepali N. Tukaye,
SangHo Kwon,
Wiliam B. Guggino
Publication year - 2013
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000343357
Subject(s) - wild type , gtpase activating protein , transfection , cell culture , chemistry , microbiology and biotechnology , biology , g protein , mutant , biochemistry , signal transduction , gene , genetics
Pseudomonas aeruginosa (PA) infections account for a large percentage of fatal hospital acquired pneumonias. One of the PA Type III secreted toxin (TTST) ExoS, a bifunctional protein with N-terminal GTPase activating protein (GAP) and C-terminal ADP rybosyl transferase (ADPRT) activities, significantly contributes to PA virulence by targeting small molecular weight G-proteins (SMWGP). In this study, we have looked at one of the mechanisms by which the GAP portion of ExoS (ExoS-GAP) mediates cellular toxicity.
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