AbstractAssembly of SNARE proteins into quaternary complexes is a critical step in membrane docking and fusion. Here, we have studied the influence of the transmembrane segments on formation of the late endosomal SNARE complex. The complex was assembled in vitro from full-length recombinant SNAREs and from mutants, where the transmembrane segments were either deleted or replaced by oligo-alanine sequences. We show that endobrevin, syntaxin 7, syntaxin 8, and vti1b readily form a complex. This complex forms a dimer as well as multimeric structures. Interestingly, the natural transmembrane segments accelerate the conversion of the quaternary complex to the dimeric form and are essential for multimerization. These in vitro results suggest that...
In the early secretory pathway newly synthesized proteins are transported sequentially through the e...
SNAREs (soluble N-ethylmaleimide-sensitive factor attachment receptors) represent an evolutionarily ...
SNARE complexes are required for membrane fusion in the endomembrane system. They contain coiled-coi...
AbstractAssembly of SNARE proteins into quaternary complexes is a critical step in membrane docking ...
SNARE proteins are crucial for intracellular membrane fusion in all eukaryotes. These proteins assem...
AbstractEukaryotic cells distribute materials among intracellular organelles and secrete into the ex...
SNARE proteins are crucial for intracellular membrane fusion in all eukaryotes. These proteins assem...
SNARE proteins are crucial for intracellular membrane fusion in all eukaryotes. These proteins assem...
Both heterotypic and homotypic fusion events are required to deliver endocytosed macromolecules to l...
Both heterotypic and homotypic fusion events are required to deliver endocytosed macromolecules to l...
AbstractA conserved molecular machinery based on SNARE proteins catalyzes most, if not all, cellular...
AbstractSNARE proteins function at the center of membrane fusion reactions by forming complexes with...
AbstractThe structure of the core of the neuronal ‘SNARE complex’, involved in neurotransmitter rele...
Formation of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) compl...
SNARE complexes are required for membrane fusion in the endomembrane system. They contain coiled-coi...
In the early secretory pathway newly synthesized proteins are transported sequentially through the e...
SNAREs (soluble N-ethylmaleimide-sensitive factor attachment receptors) represent an evolutionarily ...
SNARE complexes are required for membrane fusion in the endomembrane system. They contain coiled-coi...
AbstractAssembly of SNARE proteins into quaternary complexes is a critical step in membrane docking ...
SNARE proteins are crucial for intracellular membrane fusion in all eukaryotes. These proteins assem...
AbstractEukaryotic cells distribute materials among intracellular organelles and secrete into the ex...
SNARE proteins are crucial for intracellular membrane fusion in all eukaryotes. These proteins assem...
SNARE proteins are crucial for intracellular membrane fusion in all eukaryotes. These proteins assem...
Both heterotypic and homotypic fusion events are required to deliver endocytosed macromolecules to l...
Both heterotypic and homotypic fusion events are required to deliver endocytosed macromolecules to l...
AbstractA conserved molecular machinery based on SNARE proteins catalyzes most, if not all, cellular...
AbstractSNARE proteins function at the center of membrane fusion reactions by forming complexes with...
AbstractThe structure of the core of the neuronal ‘SNARE complex’, involved in neurotransmitter rele...
Formation of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) compl...
SNARE complexes are required for membrane fusion in the endomembrane system. They contain coiled-coi...
In the early secretory pathway newly synthesized proteins are transported sequentially through the e...
SNAREs (soluble N-ethylmaleimide-sensitive factor attachment receptors) represent an evolutionarily ...
SNARE complexes are required for membrane fusion in the endomembrane system. They contain coiled-coi...