Nuclear pore complexes (NPCs) mediate nucleocytoplasmic transport. Their intricate 120 MDa architecture remains incompletely understood. Here, we report a near-complete structural model of the human NPC scaffold with explicit membrane and in multiple conformational states. We combined AI-based structure prediction with in situ and in cellulo cryo-electron tomography and integrative modeling. We show that linker Nups spatially organize the scaffold within and across subcomplexes to establish the higher-order structure. Microsecond-long molecular dynamics simulations suggest that the scaffold is not required to stabilize the inner and outer nuclear membrane fusion, but rather widens the central pore. Our work exemplifies how AI-based modeling...
The nuclear envelope has to be reformed after mitosis to create viable daughter cells with closed nu...
Nuclear pore complexes (NPCs) perforate the double-layered nuclear envelope and form the main gatewa...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 2017Cataloged from PDF...
Nuclear pore complexes (NPCs) mediate nucleocytoplasmic transport. Their intricate 120-megadalton ar...
AbstractNuclear pore complexes (NPCs) create large conduits for cargo transport between the nucleus ...
Nuclear pore complexes (NPCs) are 110-megadalton assemblies that mediate nucleocytoplasmic transport...
The nuclear pore complex (NPC) is a fundamental component of all eukaryotic cells that facilitates n...
SummaryThe nuclear pore complex (NPC) is a fundamental component of all eukaryotic cells that facili...
Nuclear pore complexes (NPCs) perforate the nuclear envelope and represent the exclusive passageway ...
Nuclear pore complexes (NPCs) are large macromolecular machines that mediate the traffic between the...
Nuclear pore complexes (NPCs) are large macromolecular machines that mediate the traffic between the...
Nuclear pore complexes (NPCs) are proteinaceous assemblies of approximately 50 MDa that selectively ...
SummaryNuclear pore complexes (NPCs) are the sole passage through the nuclear envelope, connecting t...
Nuclear pore complexes (NPCs) are the only gateways between the nucleus and cytoplasm in eukaryotic ...
Nuclear pore complexes (NPCs) are large macromolecular machines that mediate the traffic between the...
The nuclear envelope has to be reformed after mitosis to create viable daughter cells with closed nu...
Nuclear pore complexes (NPCs) perforate the double-layered nuclear envelope and form the main gatewa...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 2017Cataloged from PDF...
Nuclear pore complexes (NPCs) mediate nucleocytoplasmic transport. Their intricate 120-megadalton ar...
AbstractNuclear pore complexes (NPCs) create large conduits for cargo transport between the nucleus ...
Nuclear pore complexes (NPCs) are 110-megadalton assemblies that mediate nucleocytoplasmic transport...
The nuclear pore complex (NPC) is a fundamental component of all eukaryotic cells that facilitates n...
SummaryThe nuclear pore complex (NPC) is a fundamental component of all eukaryotic cells that facili...
Nuclear pore complexes (NPCs) perforate the nuclear envelope and represent the exclusive passageway ...
Nuclear pore complexes (NPCs) are large macromolecular machines that mediate the traffic between the...
Nuclear pore complexes (NPCs) are large macromolecular machines that mediate the traffic between the...
Nuclear pore complexes (NPCs) are proteinaceous assemblies of approximately 50 MDa that selectively ...
SummaryNuclear pore complexes (NPCs) are the sole passage through the nuclear envelope, connecting t...
Nuclear pore complexes (NPCs) are the only gateways between the nucleus and cytoplasm in eukaryotic ...
Nuclear pore complexes (NPCs) are large macromolecular machines that mediate the traffic between the...
The nuclear envelope has to be reformed after mitosis to create viable daughter cells with closed nu...
Nuclear pore complexes (NPCs) perforate the double-layered nuclear envelope and form the main gatewa...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 2017Cataloged from PDF...