核局在化シグナルとインポート

Nuclear localization signals (NLS) are short stretches of amino acid sequences that mark proteins for nuclear import. Proteins destined for the nucleus contain these signals, which are recognized by specialized import receptors called importins. Without NLS, proteins cannot be directed to and transported across the nuclear envelope.

Importin alpha recognizes and binds the NLS of cargo proteins, forming a cargo-receptor complex. Importin beta then binds to cytoplasmic fibrils extending from the nuclear pore complex and docks the cargo-receptor complex at the channel opening. Together, these subunits facilitate transport of the cargo protein into the nucleus.

The inner channel of the nuclear pore complex is lined with phenylalanine-glycine (FG) repeats that form a gel-like selective barrier. As the cargo-receptor complex moves through, the importin beta subunit makes weak contacts with these FG repeats and hops across the channel, dissolving the gel-like barrier and allowing passage of the cargo protein.

Classical NLS exist in two forms: monopartite and bipartite. Monopartite NLS consists of a single cluster of 4-8 amino acids rich in lysine and arginine. Bipartite NLS contains two clusters of 2-3 amino acids separated by a 9-12 residue proline-rich linker. Both types are recognized by importin alpha for nuclear targeting.

Once inside the nucleus, the GTP-bound protein Ran binds to importin beta and induces a conformational change in the receptor. This conformational change causes the importin alpha-cargo complex to dissociate, releasing the cargo protein into the nucleus. The importin-Ran-GTP complex is then transported back to the cytosol for recycling.

When the importin-Ran-GTP complex returns to the cytosol, GTP is hydrolyzed to GDP, releasing the importins. The freed importin alpha and beta subunits dissociate and become available as soluble dimers in the cytosol for another round of cargo import, enabling continuous nuclear protein transport.

Beyond classical monopartite and bipartite NLS, cells use non-classical NLS, putative NLS, spatial epitope NLS, and cryptic NLS for nuclear targeting. These alternative signal types provide flexibility in protein recognition and allow importins to transport diverse cargo proteins. Some proteins contain multiple NLS to enhance nuclear import efficiency.