AbstractDespite the considerable information available with regards to the structure of the clostridial neurotoxins, and their inherent threat as biological warfare agents, the mechanisms underpinning their interactions with and translocation through the cell membrane remain poorly understood. We report herein the results of an in situ scanning probe microscopy study of the interaction of tetanus toxin C-fragment (Tet C) with supported planar lipid bilayers containing the ganglioside receptor GT1b. Our results show that Tet C preferentially binds to the surface of fluid phase domains within biphasic membranes containing GT1b and that with an extended incubation period these interactions lead to dramatic changes in the morphology of the lipi...
The orientation of cholera toxin bound to its cell-surface receptor, ganglioside GM1, in a supportin...
The entry of tetanus neurotoxin into neuronal cells proceeds through the initial binding of the toxi...
Tetanus and botulinum neurotoxins are di-chain proteins that cause paralysis by inhibiting neuroexoc...
AbstractDespite the considerable information available with regards to the structure of the clostrid...
AbstractThe interaction of Tetunus toxin with phospholipid vesicles containing gangliosides (GD1a, G...
We investigated the interaction of tetanus toxin with small unilamellar vesicles composed of differe...
The goal of this project was to clarify the mechanism of action of Clostridium tetani toxin through...
Tetanus toxin, a member of the family of Clostridial neurotoxins, is one of the most potent toxins k...
Cholera toxin which binds specifically and with high affinity to a glycolipid; ganglioside GM1, has ...
The binding properties of cholera toxin B (CTB) oligomer to substrate supported membrane bilayer, co...
It is important to understand the physicochemical mechanisms that are responsible for the morphologi...
The Clostridial neurotoxins, botulinum and tetanus, gain entry into motor neurons by binding to the ...
Summary Tetanus and botulinum neurotoxins are di-chain proteins that cause paralysis by inhibit...
A detailed characterization of the properties of the channel formed by tetanus toxin in planar lipid...
Cholera toxin is a highly efficient biotoxin, which is frequently used as a tool to investigate prot...
The orientation of cholera toxin bound to its cell-surface receptor, ganglioside GM1, in a supportin...
The entry of tetanus neurotoxin into neuronal cells proceeds through the initial binding of the toxi...
Tetanus and botulinum neurotoxins are di-chain proteins that cause paralysis by inhibiting neuroexoc...
AbstractDespite the considerable information available with regards to the structure of the clostrid...
AbstractThe interaction of Tetunus toxin with phospholipid vesicles containing gangliosides (GD1a, G...
We investigated the interaction of tetanus toxin with small unilamellar vesicles composed of differe...
The goal of this project was to clarify the mechanism of action of Clostridium tetani toxin through...
Tetanus toxin, a member of the family of Clostridial neurotoxins, is one of the most potent toxins k...
Cholera toxin which binds specifically and with high affinity to a glycolipid; ganglioside GM1, has ...
The binding properties of cholera toxin B (CTB) oligomer to substrate supported membrane bilayer, co...
It is important to understand the physicochemical mechanisms that are responsible for the morphologi...
The Clostridial neurotoxins, botulinum and tetanus, gain entry into motor neurons by binding to the ...
Summary Tetanus and botulinum neurotoxins are di-chain proteins that cause paralysis by inhibit...
A detailed characterization of the properties of the channel formed by tetanus toxin in planar lipid...
Cholera toxin is a highly efficient biotoxin, which is frequently used as a tool to investigate prot...
The orientation of cholera toxin bound to its cell-surface receptor, ganglioside GM1, in a supportin...
The entry of tetanus neurotoxin into neuronal cells proceeds through the initial binding of the toxi...
Tetanus and botulinum neurotoxins are di-chain proteins that cause paralysis by inhibiting neuroexoc...