A toolkit to study nuclear transport pathways: nanobody-mediated inhibition of importin β-related nuclear transport receptors (NTRs)
Seiten
2023
Cuvillier Verlag
978-3-7369-7847-8 (ISBN)
Cuvillier Verlag
978-3-7369-7847-8 (ISBN)
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Eukaryotic cells are divided into a nuclear and a cytoplasmic compartment. This separates transcription from translation and makes gene expression dependent on nucleocytoplasmic transport. The members of the importin β superfamily function as shuttling nuclear transport receptors (NTRs) that recognize and actively transport cargoes through nuclear pores. An estimated 5 000 to 10 000 different human proteins are subject to active nuclear transport. Numerous cargo/NTR pairs have been identified, however, we are still far from a complete understanding as it has been very challenging to setup a systematic in vivo analysis that integrates the impact of all transport pathways.
In this study, we obtained anti-NTR nanobodies against TRN1, Xpo4, Xpo7, and CAS. Our aim was to identify nanobodies, and prepare nanobody fusions, that impede nuclear pore-passage of the targeted NTR and thus, interrupt a given transport cycle. These nanobody fusions were observed to inhibit the partition of NTR/cargo complexes into a reconstituted FG phase. We also observed that the nanobodies and nanobody fusions inhibit NTR transport in permeabilized cells.
Eukaryotic cells are divided into a nuclear and a cytoplasmic compartment. This separates transcription from translation and makes gene expression dependent on nucleocytoplasmic transport. The members of the importin β superfamily function as shuttling nuclear transport receptors (NTRs) that recognize and actively transport cargoes through nuclear pores. An estimated 5 000 to 10 000 different human proteins are subject to active nuclear transport. Numerous cargo/NTR pairs have been identified, however, we are still far from a complete understanding as it has been very challenging to setup a systematic in vivo analysis that integrates the impact of all transport pathways.
In this study, we obtained anti-NTR nanobodies against TRN1, Xpo4, Xpo7, and CAS. Our aim was to identify nanobodies, and prepare nanobody fusions, that impede nuclear pore-passage of the targeted NTR and thus, interrupt a given transport cycle. These nanobody fusions were observed to inhibit the partition of NTR/cargo complexes into a reconstituted FG phase. We also observed that the nanobodies and nanobody fusions inhibit NTR transport in permeabilized cells.
Erscheinungsdatum | 16.08.2023 |
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Verlagsort | Göttingen |
Sprache | englisch |
Maße | 148 x 210 mm |
Themenwelt | Naturwissenschaften ► Biologie ► Biochemie |
Naturwissenschaften ► Biologie ► Genetik / Molekularbiologie | |
Technik ► Umwelttechnik / Biotechnologie | |
Schlagworte | biportins, export complex • CAS, nanobody fusions • eukaryotic cells, nucleus, compartmentalization • Exportin 4 (Xpo4), Exportin 7 (Xpo7) • impede nuclear pore passage • importin, shuttling, nuclear transport receptors (NTRs) • Inhibition • Kernporenkomplex (NPC) • Kerntransportrezeptoren (NTRs) • Nanokörperfusionen, NTR-vermeideter Transport • NTR blockers, eukaryotische Zellen • NTR/cargo complexes, FG phase • NTR-meidated transport • nuclear pore complex (NPC), importins, exportins • nucleocytoplasmic transport • nucleoporins (Nups), tag-Nbs • nukleozytoplasmatischer Transport • permeabilisierte Zellen, NTR-Blocker • permeabilized cells, Ran binding • transport block, nanobodies (Nbs) • transport cycle, inhibitor • Transportin 1 (TRN1) • transport pathways, anti-NTR nanobodies • Zellkern, Kompartimentierung |
ISBN-10 | 3-7369-7847-2 / 3736978472 |
ISBN-13 | 978-3-7369-7847-8 / 9783736978478 |
Zustand | Neuware |
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