نتایج جستجو برای: cholera toxin subunit b

تعداد نتایج: 1022123  

2011
Gunasagaran Shamini Manickam Ravichandran John T Sinnott Charurut Somboonwit Harcharan S Sidhu Paul Shapshak Pandjassarame Kangueane

Cholera is a global disease that has persisted for millennia. The cholera toxin (CT) from Vibrio cholerae is responsible for the clinical symptoms of cholera. This toxin is a hetero-hexamer (AB(5)) complex consisting of a subunit A (CTA) with a pentamer (B(5)) of subunit B (CTB). The importance of the AB(5) complex for pathogenesis is established for the wild type O1 serogroup using known struc...

Journal: :The British journal of ophthalmology 1997
D Ma J Mellon J Y Niederkorn

AIMS To determine optimal conditions for enhancing corneal allograft survival through oral administration of donor specific corneal cells. METHODS A mouse model of penetrating keratoplasty was used to evaluate the efficacy and optimal conditions for preventing immunological rejection of corneal allografts. C3H corneal grafts were transplanted orthotopically to CB6F1 recipients and represented...

Journal: :Microbiology 1997
B Stentebjerg-Olesen L Pallesen L B Jensen G Christiansen P Klemm

The potential of the major structural protein of type 1 fimbriae as a display system for heterologous sequences was tested. As a reporter-epitope, a heterologous sequence mimicking a neutralizing epitope of the cholera toxin B chain was inserted, in one or two copies, into four different positions in the fimA gene. This was carried out by introduction of new restriction sites by PCR-mediated si...

2012
Charles A. Day Anne K. Kenworthy

Multivalent glycolipid binding toxins such as cholera toxin have the capacity to cluster glycolipids, a process thought to be important for their functional uptake into cells. In contrast to the highly dynamic properties of lipid probes and many lipid-anchored proteins, the B-subunit of cholera toxin (CTxB) diffuses extremely slowly when bound to its glycolipid receptor GM(1) in the plasma memb...

2012
Michael G. Jobling ZhiJie Yang Wendy R. Kam Wayne I. Lencer Randall K. Holmes

Cholera toxin (CT) from Vibrio cholerae is responsible for the majority of the symptoms of the diarrheal disease cholera. CT is a heterohexameric protein complex with a 240-residue A subunit and a pentameric B subunit of identical 103-residue B polypeptides. The A subunit is proteolytically cleaved within a disulfide-linked loop to generate the A1 and A2 fragments. The B subunit of wild-type (w...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1982
J J Mekalanos S L Moseley J R Murphy S Falkow

Phenotypically nontoxinogenic mutants of Vibrio cholerae were isolated after infection with either of two mutagenic vibriophages, VcAI and VcA2ctsl. DNA isolated from these mutants was analyzed for toxin gene sequences by the Southern blotting method with 32P-labeled probes derived from the cloned A and B subunit genes for the heat-labile enterotoxin of Escherichia coli, designated LT. Several ...

Journal: :Molecular biology of the cell 2003
Yukako Fujinaga Anne A Wolf Chiara Rodighiero Heidi Wheeler Billy Tsai Larry Allen Michael G Jobling Tom Rapoport Randall K Holmes Wayne I Lencer

Cholera toxin (CT) travels from the plasma membrane of intestinal cells to the endoplasmic reticulum (ER) where a portion of the A-subunit, the A1 chain, crosses the membrane into the cytosol to cause disease. A related toxin, LTIIb, binds to intestinal cells but does not cause toxicity. Here, we show that the B-subunit of CT serves as a carrier for the A-subunit to the ER where disassembly occ...

Journal: :The Biochemical journal 1991
F R McKenzie G Milligan

Cholera toxin treatment (up to 1 microgram/ml, 16 h) of neuroblastoma x glioma hybrid NG108-15 cells produced a decrease of some 35% in both delta opioid receptor-mediated stimulation of high-affinity GTPase activity and inhibition of forskolin-amplified adenylate cyclase. Coincident with these decreases was a down-regulation of some 35% in the delta opioid receptor population. A similar patter...

Journal: :Infection and immunity 2004
Richard Malley Sarah C Morse Luciana C C Leite Ana Paula Mattos Areas Paulo Lee Ho Flavia S Kubrusly Igor C Almeida Porter Anderson

Intranasal challenge of C57BL/6 mice with Streptococcus pneumoniae serotypes 6B, 14, and 23F produced colonization of the middle ear and NP. Intranasal vaccination with ethanol-killed nonencapsulated cells with adjuvant protected both sites. Of four nontoxic adjuvants tested, the cholera toxin B subunit was most effective and least nonspecifically protective.

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