TY - JOUR
T1 - Characterization of Fluorescent Chimeras of Cholera Toxin and Escherichia coli Heat-Labile Enterotoxins Produced by Use of the Twin Arginine Translocation System
AU - Tinker, Juliette K.
AU - Erbe, Jarrod L.
AU - Holmes, Randall K.
PY - 2005/6/1
Y1 - 2005/6/1
N2 - Cholera toxin (CT) is an AB 5 toxin responsible for the profusesecretory diarrhea resulting from Vibrio cholerae infection.CT consists of a pentameric, receptor-binding B subunit (CTB)and a monomeric A subunit (CTA) that has latent enzymatic activity.In addition to its enterotoxicity, CT has potent mucosal adjuvantactivity and can also function as a carrier molecule with manypotential applications in cell biology. In earlier studies,the toxic CTA 1 domain was replaced by several other antigenicprotein domains to produce holotoxin-like chimeras for use aspotential mucosal vaccines. In the present study we utilizedthe twin arginine translocation ( tat ) system to produce fluorescentCT chimeras, as well as fluorescent chimeras of Escherichiacoli heat-labile toxins LTI and LTIIb. Fusion proteins containingeither green fluorescent protein (GFP) or monomeric red fluorescentprotein (mRFP) and the A 2 domain of CT, LTI, or LTIIb were transportedto the periplasm of E. coli by the tat system, and the correspondingB polypeptides of CT, LTI, and LTIIb were transported to theperiplasm by the sec system. The fluorescent fusion proteinswere shown to assemble spontaneously and efficiently with thecorresponding B polypeptides in the periplasm to form chimericholotoxin-like molecules, and these chimeras bound to and enteredcultured cells in a manner similar to native CT, LTI, or LTIIb.The GFP and mRFP derivatives of CT, LT, and LTIIb developedhere are useful tools for studies on the cell biology of traffickingof the CT/LT family of bacterial enterotoxins. In addition,these constructs provide proof in principle for the developmentof novel chimeric CT-like or LT-like vaccine candidates containingCTA 2 fusion proteins that cannot be delivered to the periplasmof E. coli by use of the sec secretion pathway.
AB - Cholera toxin (CT) is an AB 5 toxin responsible for the profusesecretory diarrhea resulting from Vibrio cholerae infection.CT consists of a pentameric, receptor-binding B subunit (CTB)and a monomeric A subunit (CTA) that has latent enzymatic activity.In addition to its enterotoxicity, CT has potent mucosal adjuvantactivity and can also function as a carrier molecule with manypotential applications in cell biology. In earlier studies,the toxic CTA 1 domain was replaced by several other antigenicprotein domains to produce holotoxin-like chimeras for use aspotential mucosal vaccines. In the present study we utilizedthe twin arginine translocation ( tat ) system to produce fluorescentCT chimeras, as well as fluorescent chimeras of Escherichiacoli heat-labile toxins LTI and LTIIb. Fusion proteins containingeither green fluorescent protein (GFP) or monomeric red fluorescentprotein (mRFP) and the A 2 domain of CT, LTI, or LTIIb were transportedto the periplasm of E. coli by the tat system, and the correspondingB polypeptides of CT, LTI, and LTIIb were transported to theperiplasm by the sec system. The fluorescent fusion proteinswere shown to assemble spontaneously and efficiently with thecorresponding B polypeptides in the periplasm to form chimericholotoxin-like molecules, and these chimeras bound to and enteredcultured cells in a manner similar to native CT, LTI, or LTIIb.The GFP and mRFP derivatives of CT, LT, and LTIIb developedhere are useful tools for studies on the cell biology of traffickingof the CT/LT family of bacterial enterotoxins. In addition,these constructs provide proof in principle for the developmentof novel chimeric CT-like or LT-like vaccine candidates containingCTA 2 fusion proteins that cannot be delivered to the periplasmof E. coli by use of the sec secretion pathway.
UR - https://scholarworks.boisestate.edu/bio_facpubs/197
UR - http://dx.doi.org/10.1128/IAI.73.6.3627-3635.2005
UR - http://www.scopus.com/inward/record.url?scp=19744375740&partnerID=8YFLogxK
U2 - 10.1128/IAI.73.6.3627-3635.2005
DO - 10.1128/IAI.73.6.3627-3635.2005
M3 - Article
C2 - 15908392
VL - 73
SP - 3627
EP - 3635
JO - History Faculty Publications and Presentations
JF - History Faculty Publications and Presentations
IS - 6
ER -