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Sodium Bile Salt Co-Transporting Protein

spinqualitylabelsall models Sodium Bile Salt Co-Transporting Polypeptide (NTCP) with green bile salts and yellow sodium ions bound PDB: 7zyi Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Introduction Fig.1 Taruocholic acid a crystalline bile acid Shown here is the structure in a line representation of taruocholic acid with stereochemistry and important hydrogens. Sodium Taurocholate Co-Transporting Polypeptide, or NTCP, is a membrane transporter protein that is found in the plasma membrane of liver cells, or hepatocytes. NTCP's primary function is the transportation of taurocholates, or bile salts, (Fig. 1) into the liver and out of the liver to the small intestine. Bile salts play various roles in metabolism and digestion, but their main function is the emulsification of lipid droplets into smaller fragments. This enables lipases to break down the droplets into their monomers, or triglycerides which are then able to be digested. NTCP is part of the solute carrier superfamily, more specifically SLC10. NTCP is the founding member of the SLC10 family, first discovered in rat hepatocytes in 1978. NTCP has a key role in Enterohepatic circulation or bile salt recycling, and its unique ability to transport other solutes lends it therapeutic potential for lowering cholesterol and treating liver disease. NTCP also serves as a binding site for hepatitis B virus and hepatitis D virus. Future studies into HBV binding mechanism can help understand infection pathways and the development of viral inhibitors. Structure Binding Sites Sodium NTCP, like other SLC10 family members, have two sodium binding sites. Many polar and negatively charged residues (68, 105, 106, 119, 123, 257, 261) form ion-dipole or dipole-dipole interactions with the sodium ions in these sites with a high level of conservation, suggesting sodium binding is coupled to bile salt transport. Mutations in the X-motif near sodium binding sites also inhibit bile salt transport function, suggesting that sodium is required for salt binding. Thermodynamically favorable sodium transport facilitates changes in NTCP from open-pore to closed-pore states, moving bile salts against their concentration gradient. The inward-facing state is favored in the absence of sodium ions, while open-pore state is favored in the presence of sodium ions. Gating of the channel with sodium in this way allows for sodium concentrations to regulate uptake of taurocholates. When intracellular sodium levels are higher, open-pore state is favored allowing for the diffusion of taurocholates. However, when extracellular sodium levels are high, inward-facing state is favored preventing diffusion of taurocholates. Bile Salt A key feature of NTCP is its amphipathic pore which allows for bile salt transport across the hydrophilic membrane. The pore surface remains Hydrophobic, while the lining of the open pore is largely Polar. In the inward-facing or closed-pore conformation, the polar pore residues are inaccessible. Only the surface hydrophobic residues are exposed. As the pore opens up, inner polar residues become accessible allowing for the binding of hydrophilic bile salts. The pattern of hydrophobic and polar residues within the pore matches the amphipathic patterns within taurocholates, steroids, and thyroid hormones. Using this amphipathic pore, provides the channel with specificity while preventing leakage of other substrates. Essential bile salt binding residues form Van der Waals interactions with bile salt substrates, while others form dipole-dipole or ionic interactions. The core domain contributes most of the polar domains, while the panel domain contributes mainly hydrophobic surface. Conformational Change Fig. 3 NTCP shown as cartoons with panel (red) and core (blue) domains colored. Helices are moving from open-pore to inward-facing conformation (7PQQ to 7PQG) Fig. 4 NTCP surface representation with panel (red) and core (blue) domains colored. Domains are moving from open-pore to inward-facing conformation (7PQQ to 7PQG) NTCP utilizes an elevator-alternating mechanism where one domain (core) does most of the translocation, and the other domain (panel) remains stationary. Bile Salt Transport Fig. 5 Proposed process of NTCP bile salt transport. NTCP structure is shown in light blue with a white channel going through the protein. Sodium ions as yellow spheres and bile salts as green blobs with inner and outer binding sites labeled. Captions below each image detail how movement leads to transport of bile salts and conformational changes in NTCP throughout the different steps of the process. A proposed pathway for NTCP bile salt transport starting and ending with open-pore states hypothesizes that both sodium ions are translocated with the transport of one bile salt.. Only one taurocholate is transported at a time due to NTCP's two bile salt binding sites. An inner bile salt that is closer to the cytoplasmic side of the membrane and an outer bile salt that is closer to the extracellular side of the membrane In the open-pore state both taurocholates and sodium ions bound then both sodium ions are released into the cytoplasm along with the inner bile salt into the cytoplasm (Fig. 5). The outermost bile salt remains bound in the pore, likely helping to prevent leakage. The outer bile salt is displaced into the inner bile salt binding site by the movement of sodium ions, this displacement then facilitates the conformational change to the inward-facing, pore inaccessible conformation (Fig. 5). Sodium ions then bind to NTCP, favoring the open-pore state and also allowing for the binding of another outer bile salt (Fig 5). The protein is then reset and the process can then start again releasing the next inner bile salt with the translocation of the sodium ions into the cytoplasm. This mechanism melds typical patterns of gated channels and pumps in a new light as sodium ions control conformation and thus binding, displacement, and release of bile salts. HBV Binding and Infection NTCP is the only entry receptor into the liver for HBV and HDV. These viruses are known to use two different patches (residues 84-87 and 157-165) on NTCP for binding and entry. The myristolated PreS1 domain of HBV binds to NTCP through the first hydrophobic patch on NTCP containing residues 157-165 on the open pore surface. These residues form part of the bile salt transport tunnel resulting in HBV binding and bile salt transport directly competing and interfering with one another. The other hydrophobic patch consisting of residues 84-87 found on the N-terminus of NTCP does not overlap with bile salt binding and may be used for the development of antivirals that do not inhibit bile uptake . Other minor variations within NTCP provide species specificity for HBV or virus resistance, such as mutant S267F found in East Asia. [EXPLAIN HOW GIVES RESISTANCE] The exact mechanism by which NTCP mediates viral internalization is still being determined; however, current evidence suggests it works through endocytosis. Once HBV is bound, the NTCP/HBV complex is taken into the cell where viral contents are dumped into the cytoplasm to then begin viral replication. HBV may also interact with other receptors or host cell factors, but NTCP alone is not sufficient for infection.